Literature DB >> 21578768

6-Butyl-5-(4-methoxy-phen-oxy)-3-phenyl-3H-1,2,3-triazolo[4,5-d]pyrimidin-7(6H)-one.

Xiao-Hua Zeng, Shou-Heng Deng, Ping Chen, Hong-Mei Wang, Zuan Ma.   

Abstract

The asymmetric unit of the title compound, C(21)H(21)N(5)O(3), consists of two geometrically similar mol-ecules. The fused rings of the triazolo[4,5-d]pyrimidine system are nearly coplanar, making dihedral angels of 1.48 (18) and 1.34 (16)°, and the n class="Chemical">phenyl rings are twisted by 12.3 (1) and 8.7 (1)° with respect to the triazolopyrimidine plane. The ethyl groups of the n-butyl side chains are disordered over two sites in each of the independent mol-ecules, the ratios of occupancies being 0.60:0.40 and 0.61:0.39.

Entities:  

Year:  2009        PMID: 21578768      PMCID: PMC2971827          DOI: 10.1107/S1600536809046017

Source DB:  PubMed          Journal:  Acta Crystallogr Sect E Struct Rep Online        ISSN: 1600-5368


Related literature

For the biological activity of 8-aza­guanine derivatives, see: Roblin et al. (1945 ▶); Ding et al. (2004 ▶); Mitchell et al. (1950 ▶); Levine et al. (1963 ▶); Montgomery et al. (1962 ▶)); Yamamoto et al. (1967 ▶); Bariana (1971 ▶); Holland et al. (1975 ▶). For related structures, see: Wang et al. (2006 ▶); Zeng et al. (2006 ▶, 2009 ▶); Zhao, Hu et al. (2005 ▶); Zhao, Wang & n class="Gene">Ding (2005 ▶); Zhao, Xie et al. (2005 ▶).

Experimental

Crystal data

C21H21N5O3 M = 391.43 Triclinic, a = 11.5167 (13) Å b = 12.4026 (13) Å c = 14.9353 (16) Å α = 78.795 (2)° β = 76.207 (2)° γ = 76.360 (2)° V = 1991.7 (4) Å3 Z = 4 Mo Kα radiation μ = 0.09 mm−1 T = 298 K 0.15 × 0.12 × 0.10 mm

Data collection

Bruker SMART CCD area-detector diffractometer Absorption correction: multi-scan (SADABS; Sheldrick, 1996 ▶) T min = 0.987, T max = 0.991 11898 measured reflections 6940 independent reflections 5252 reflections with I > 2σ(I) R int = 0.061

Refinement

R[F 2 > 2σ(F 2)] = 0.079 wR(F 2) = 0.212 S = 1.07 6940 reflections 567 parameters 12 restraints H-atom parameters constrained Δρmax = 0.44 e Å−3 Δρmin = −0.22 e Å−3 Data collection: SMART (Bruker, 2001 ▶); cell refinement: SAINT (Bruker, 2001 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: PLATON (Spek, 2009 ▶); software used to prepare material for publication: SHELXTL97 (Sheldrick, 2008 ▶). Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536809046017/ya2108sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536809046017/ya2108Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C21H21N5O3Z = 4
Mr = 391.43F(000) = 824
Triclinic, P1Dx = 1.305 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 11.5167 (13) ÅCell parameters from 4234 reflections
b = 12.4026 (13) Åθ = 2.3–25.4°
c = 14.9353 (16) ŵ = 0.09 mm1
α = 78.795 (2)°T = 298 K
β = 76.207 (2)°Block, colorless
γ = 76.360 (2)°0.15 × 0.12 × 0.10 mm
V = 1991.7 (4) Å3
Bruker SMART CCD area-detector diffractometer6940 independent reflections
Radiation source: fine-focus sealed tube5252 reflections with I > 2σ(I)
graphiteRint = 0.061
φ and ω scansθmax = 25.0°, θmin = 2.0°
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)h = −13→13
Tmin = 0.987, Tmax = 0.991k = −13→14
11898 measured reflectionsl = −17→17
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.079Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.212H-atom parameters constrained
S = 1.07w = 1/[σ2(Fo2) + (0.0878P)2 + 0.7377P] where P = (Fo2 + 2Fc2)/3
6940 reflections(Δ/σ)max < 0.001
567 parametersΔρmax = 0.44 e Å3
12 restraintsΔρmin = −0.22 e Å3
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.
Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.
xyzUiso*/UeqOcc. (<1)
C10.3813 (3)1.1282 (3)−0.0630 (2)0.0704 (8)
C20.4159 (3)1.2053 (3)−0.1390 (3)0.0929 (11)
H20.44731.2648−0.13150.112*
C30.4038 (4)1.1937 (4)−0.2255 (3)0.1134 (15)
H30.42861.2451−0.27670.136*
C40.3560 (4)1.1082 (4)−0.2378 (3)0.1053 (13)
H40.34691.1021−0.29680.126*
C50.3215 (3)1.0312 (3)−0.1625 (3)0.0918 (10)
H50.28970.9721−0.17030.110*
C60.3341 (3)1.0418 (3)−0.0745 (2)0.0789 (9)
H60.31030.9900−0.02330.095*
C70.3573 (3)1.0900 (2)0.1139 (2)0.0642 (7)
C80.4017 (3)1.1368 (3)0.1700 (3)0.0748 (8)
C90.3731 (3)1.1058 (3)0.2691 (3)0.0856 (10)
C100.2607 (3)0.9846 (3)0.2292 (2)0.0708 (8)
C110.1502 (3)0.8491 (3)0.2166 (2)0.0695 (8)
C120.0289 (3)0.8462 (3)0.2362 (2)0.0759 (9)
H12−0.02570.89300.27580.091*
C13−0.0129 (3)0.7744 (3)0.1976 (2)0.0775 (9)
H13−0.09550.77210.21100.093*
C140.0688 (3)0.7057 (3)0.1388 (2)0.0732 (8)
C150.1902 (3)0.7121 (3)0.1176 (2)0.0810 (9)
H150.24470.66760.07610.097*
C160.2326 (3)0.7834 (3)0.1569 (2)0.0767 (9)
H160.31490.78670.14320.092*
C17−0.0777 (4)0.6012 (4)0.1313 (3)0.1118 (14)
H17A−0.08690.57410.19690.168*
H17B−0.08480.54380.09930.168*
H17C−0.14010.66630.12120.168*
C180.2467 (5)0.9939 (4)0.3997 (3)0.1173 (14)
H18A0.23511.05820.43120.141*
H18B0.16820.97320.40840.141*
C190.3312 (5)0.9008 (5)0.4395 (3)0.1241 (15)
H19A0.40720.92470.43420.149*0.60
H19B0.34850.84010.40300.149*0.60
H19C0.41330.91430.42920.149*0.40
H19D0.33210.82930.42180.149*0.40
C200.2846 (11)0.8550 (9)0.5437 (5)0.121 (4)0.60
H20A0.20180.84350.55310.145*0.60
H20B0.33630.78400.56190.145*0.60
C210.2888 (10)0.9402 (8)0.5999 (5)0.132 (3)0.60
H21A0.36350.96710.57680.198*0.60
H21B0.28460.90680.66390.198*0.60
H21C0.22091.00160.59520.198*0.60
C22−0.1449 (3)0.6338 (2)0.43768 (18)0.0621 (7)
C23−0.1744 (3)0.5483 (3)0.4068 (2)0.0720 (8)
H23−0.11340.49410.37900.086*
C24−0.2963 (3)0.5440 (3)0.4179 (2)0.0820 (9)
H24−0.31690.48660.39670.098*
C25−0.3869 (3)0.6231 (4)0.4594 (2)0.0891 (10)
H25−0.46850.61990.46630.107*
C26−0.3555 (4)0.7063 (4)0.4904 (3)0.1013 (12)
H26−0.41640.75990.51910.122*
C27−0.2362 (4)0.7126 (3)0.4800 (3)0.0895 (10)
H27−0.21650.77010.50160.107*
C280.0845 (3)0.5873 (2)0.37838 (19)0.0593 (7)
C290.1745 (3)0.6332 (3)0.3916 (2)0.0678 (8)
C300.2988 (3)0.5944 (3)0.3509 (3)0.0815 (10)
C310.2108 (3)0.4696 (3)0.2899 (2)0.0733 (8)
C320.1543 (3)0.3377 (3)0.2199 (2)0.0700 (8)
C330.0893 (3)0.2762 (3)0.2924 (2)0.0785 (9)
H330.09320.27810.35360.094*
C340.0188 (3)0.2120 (3)0.2740 (2)0.0786 (9)
H34−0.02630.17100.32320.094*
C350.0135 (3)0.2071 (3)0.1841 (2)0.0701 (8)
C360.0764 (3)0.2719 (3)0.1126 (2)0.0783 (9)
H360.07130.27140.05150.094*
C370.1466 (3)0.3373 (3)0.1306 (2)0.0781 (9)
H370.18870.38120.08180.094*
C38−0.0400 (5)0.1100 (4)0.0814 (3)0.1248 (17)
H38A−0.08410.17190.04540.187*
H38B−0.07170.04390.08500.187*
H38C0.04480.09720.05210.187*
C390.4370 (5)0.4412 (4)0.2681 (5)0.1387 (19)
H39A0.48980.44630.30830.166*
H39B0.43630.36260.27040.166*
C400.4816 (4)0.4881 (4)0.1756 (5)0.1389 (19)
H40A0.47370.56710.17810.167*0.61
H40B0.42200.48410.14070.167*0.61
H40C0.47480.56850.16980.167*0.39
H40D0.44170.47160.13100.167*0.39
C410.6105 (11)0.4531 (16)0.1097 (10)0.266 (13)0.61
H41A0.60560.40160.07010.319*0.61
H41B0.63610.51880.07030.319*0.61
C420.6979 (10)0.3988 (19)0.1703 (12)0.284 (11)0.61
H42A0.72160.45500.19420.427*0.61
H42B0.76870.35620.13500.427*0.61
H42C0.66050.34970.22120.427*0.61
C20'0.2534 (19)0.9186 (14)0.5406 (7)0.208 (14)0.40
H20C0.25780.99000.55570.250*0.40
H20D0.16860.91670.54460.250*0.40
C21'0.3110 (14)0.8215 (16)0.6063 (8)0.170 (7)0.40
H21D0.30360.75180.59140.255*0.40
H21E0.27000.82870.66940.255*0.40
H21F0.39570.82290.59920.255*0.40
C41'0.6174 (7)0.4221 (14)0.1683 (10)0.131 (6)0.39
H41C0.65260.43620.21670.157*0.39
H41D0.62140.34210.17430.157*0.39
C42'0.6838 (12)0.4652 (15)0.0738 (11)0.174 (8)0.39
H42D0.64760.45080.02680.261*0.39
H42E0.76800.42790.06510.261*0.39
H42F0.67850.54450.06890.261*0.39
N10.3984 (2)1.1397 (2)0.0256 (2)0.0718 (7)
N20.4667 (3)1.2151 (2)0.0314 (3)0.0924 (9)
N30.4686 (3)1.2126 (2)0.1183 (3)0.0922 (9)
N40.2861 (2)1.0120 (2)0.13914 (17)0.0651 (6)
N50.2979 (3)1.0252 (2)0.29391 (19)0.0853 (8)
N6−0.0203 (2)0.64224 (19)0.42687 (15)0.0627 (6)
N70.0072 (3)0.7202 (2)0.46881 (18)0.0786 (8)
N80.1237 (3)0.7147 (2)0.44767 (18)0.0818 (8)
N90.0976 (2)0.50531 (19)0.32598 (16)0.0607 (6)
N100.3093 (2)0.5042 (2)0.3012 (2)0.0888 (9)
O10.4041 (3)1.1411 (2)0.3284 (2)0.1146 (9)
O20.1887 (2)0.9109 (2)0.26967 (15)0.0907 (7)
O30.3883 (2)0.6278 (2)0.3538 (2)0.1099 (9)
O40.2423 (2)0.3919 (2)0.23281 (19)0.0926 (7)
O50.0382 (2)0.6299 (2)0.09702 (18)0.0975 (8)
O6−0.0535 (2)0.1350 (2)0.17288 (18)0.0985 (8)
U11U22U33U12U13U23
C10.0525 (16)0.0621 (19)0.080 (2)−0.0022 (14)−0.0041 (14)0.0059 (16)
C20.083 (2)0.082 (2)0.095 (3)−0.0164 (19)−0.0054 (19)0.016 (2)
C30.103 (3)0.118 (4)0.089 (3)−0.017 (3)−0.004 (2)0.031 (3)
C40.088 (3)0.134 (4)0.071 (2)−0.006 (3)−0.0051 (19)0.006 (2)
C50.086 (2)0.104 (3)0.075 (2)−0.012 (2)−0.0074 (18)−0.008 (2)
C60.069 (2)0.080 (2)0.072 (2)−0.0116 (17)−0.0004 (15)0.0038 (17)
C70.0537 (16)0.0508 (16)0.079 (2)−0.0017 (13)−0.0093 (14)−0.0045 (15)
C80.0682 (19)0.0572 (18)0.096 (2)−0.0068 (15)−0.0154 (17)−0.0129 (17)
C90.092 (2)0.073 (2)0.098 (3)−0.0042 (19)−0.031 (2)−0.026 (2)
C100.0747 (19)0.0667 (19)0.070 (2)−0.0118 (16)−0.0160 (15)−0.0097 (16)
C110.085 (2)0.0651 (18)0.0525 (16)−0.0167 (17)−0.0152 (15)0.0094 (14)
C120.072 (2)0.071 (2)0.0683 (19)−0.0076 (16)−0.0023 (15)0.0062 (16)
C130.0637 (19)0.084 (2)0.075 (2)−0.0144 (17)−0.0173 (16)0.0143 (18)
C140.072 (2)0.074 (2)0.0682 (19)−0.0107 (17)−0.0227 (16)0.0077 (16)
C150.074 (2)0.084 (2)0.078 (2)−0.0077 (18)−0.0110 (16)−0.0093 (18)
C160.0640 (19)0.080 (2)0.082 (2)−0.0157 (17)−0.0182 (16)0.0023 (18)
C170.113 (3)0.139 (4)0.100 (3)−0.057 (3)−0.036 (2)0.002 (3)
C180.135 (4)0.123 (4)0.108 (3)−0.033 (3)−0.042 (3)−0.021 (3)
C190.124 (4)0.139 (4)0.119 (4)−0.041 (3)−0.033 (3)−0.011 (3)
C200.171 (8)0.147 (10)0.065 (5)−0.097 (7)−0.039 (5)0.034 (5)
C210.197 (9)0.137 (8)0.071 (5)−0.052 (7)−0.016 (5)−0.029 (5)
C220.082 (2)0.0595 (17)0.0467 (14)−0.0145 (15)−0.0234 (13)0.0009 (13)
C230.081 (2)0.075 (2)0.0632 (18)−0.0214 (17)−0.0150 (15)−0.0092 (15)
C240.089 (2)0.094 (2)0.073 (2)−0.032 (2)−0.0205 (18)−0.0121 (18)
C250.075 (2)0.116 (3)0.075 (2)−0.011 (2)−0.0279 (18)−0.006 (2)
C260.088 (3)0.105 (3)0.112 (3)0.010 (2)−0.038 (2)−0.033 (2)
C270.104 (3)0.079 (2)0.096 (3)−0.007 (2)−0.040 (2)−0.027 (2)
C280.0784 (19)0.0533 (16)0.0523 (15)−0.0204 (15)−0.0306 (14)0.0081 (13)
C290.090 (2)0.0656 (18)0.0599 (17)−0.0326 (17)−0.0351 (16)0.0073 (15)
C300.086 (2)0.078 (2)0.097 (2)−0.0317 (19)−0.049 (2)0.0062 (18)
C310.068 (2)0.0630 (19)0.097 (2)−0.0120 (15)−0.0364 (17)−0.0077 (17)
C320.0551 (17)0.0622 (18)0.093 (2)−0.0032 (14)−0.0152 (15)−0.0213 (17)
C330.087 (2)0.078 (2)0.071 (2)−0.0079 (18)−0.0181 (17)−0.0196 (17)
C340.086 (2)0.081 (2)0.069 (2)−0.0279 (18)−0.0039 (16)−0.0120 (17)
C350.0668 (18)0.0706 (19)0.073 (2)−0.0176 (15)−0.0114 (15)−0.0085 (16)
C360.089 (2)0.083 (2)0.0656 (19)−0.0233 (19)−0.0201 (16)−0.0038 (17)
C370.076 (2)0.074 (2)0.080 (2)−0.0204 (17)−0.0094 (16)−0.0014 (17)
C380.166 (5)0.150 (4)0.093 (3)−0.082 (4)−0.041 (3)−0.017 (3)
C390.111 (4)0.105 (4)0.219 (7)−0.035 (3)−0.059 (4)−0.020 (4)
C400.109 (4)0.106 (4)0.202 (6)−0.027 (3)−0.032 (4)−0.015 (4)
C410.162 (15)0.182 (13)0.32 (3)0.038 (11)0.090 (15)0.014 (17)
C420.108 (9)0.44 (3)0.254 (19)0.042 (14)−0.034 (11)−0.048 (19)
C20'0.41 (4)0.164 (19)0.071 (10)−0.15 (2)−0.052 (14)0.041 (11)
C21'0.121 (11)0.22 (2)0.132 (13)−0.017 (12)0.003 (9)0.008 (13)
C41'0.044 (6)0.194 (18)0.154 (13)−0.035 (8)−0.026 (7)−0.002 (11)
C42'0.100 (11)0.192 (16)0.205 (18)−0.034 (11)0.076 (12)−0.095 (15)
N10.0600 (15)0.0578 (15)0.0877 (19)−0.0113 (12)−0.0045 (13)−0.0002 (13)
N20.082 (2)0.0746 (19)0.115 (3)−0.0258 (16)−0.0075 (17)−0.0036 (18)
N30.085 (2)0.0727 (19)0.121 (3)−0.0197 (16)−0.0201 (18)−0.0163 (18)
N40.0657 (15)0.0622 (15)0.0607 (15)−0.0086 (12)−0.0096 (11)−0.0021 (11)
N50.102 (2)0.0855 (19)0.0711 (18)−0.0220 (17)−0.0203 (15)−0.0098 (15)
N60.0871 (18)0.0588 (14)0.0496 (13)−0.0233 (13)−0.0235 (12)−0.0023 (11)
N70.111 (2)0.0760 (17)0.0627 (15)−0.0389 (16)−0.0237 (15)−0.0095 (13)
N80.117 (2)0.0825 (19)0.0650 (16)−0.0486 (18)−0.0337 (15)−0.0017 (14)
N90.0634 (15)0.0572 (14)0.0666 (14)−0.0112 (11)−0.0280 (11)−0.0040 (11)
N100.0599 (16)0.0815 (19)0.134 (3)−0.0122 (14)−0.0391 (16)−0.0159 (18)
O10.144 (3)0.103 (2)0.114 (2)−0.0306 (18)−0.0407 (18)−0.0324 (17)
O20.1180 (19)0.0982 (17)0.0616 (13)−0.0480 (16)−0.0136 (12)0.0013 (12)
O30.0943 (18)0.114 (2)0.147 (2)−0.0462 (16)−0.0537 (17)−0.0124 (18)
O40.0615 (13)0.0880 (16)0.138 (2)−0.0121 (12)−0.0179 (13)−0.0449 (16)
O50.0979 (18)0.1090 (19)0.0956 (17)−0.0366 (15)−0.0251 (14)−0.0123 (15)
O60.1103 (19)0.1090 (19)0.0899 (17)−0.0546 (16)−0.0113 (14)−0.0179 (14)
C1—C61.366 (4)C25—H250.9300
C1—C21.379 (5)C26—C271.364 (5)
C1—N11.422 (4)C26—H260.9300
C2—C31.370 (6)C27—H270.9300
C2—H20.9300C28—N61.354 (4)
C3—C41.365 (6)C28—N91.360 (4)
C3—H30.9300C28—C291.363 (4)
C4—C51.373 (5)C29—N81.373 (4)
C4—H40.9300C29—C301.422 (5)
C5—C61.390 (5)C30—O31.211 (4)
C5—H50.9300C30—N101.426 (4)
C6—H60.9300C31—N91.293 (4)
C7—C81.354 (4)C31—O41.339 (4)
C7—N41.355 (4)C31—N101.359 (4)
C7—N11.366 (4)C32—C371.359 (5)
C8—N31.360 (4)C32—C331.371 (5)
C8—C91.432 (5)C32—O41.407 (4)
C9—O11.217 (4)C33—C341.365 (4)
C9—N51.413 (5)C33—H330.9300
C10—N41.301 (4)C34—C351.373 (4)
C10—O21.339 (4)C34—H340.9300
C10—N51.363 (4)C35—O61.367 (4)
C11—C121.365 (4)C35—C361.371 (4)
C11—C161.368 (5)C36—C371.372 (4)
C11—O21.406 (4)C36—H360.9300
C12—C131.376 (5)C37—H370.9300
C12—H120.9300C38—O61.424 (5)
C13—C141.379 (5)C38—H38A0.9600
C13—H130.9300C38—H38B0.9600
C14—O51.374 (4)C38—H38C0.9600
C14—C151.376 (4)C39—C401.414 (8)
C15—C161.382 (5)C39—N101.510 (6)
C15—H150.9300C39—H39A0.9700
C16—H160.9300C39—H39B0.9700
C17—O51.413 (4)C40—C41'1.574 (9)
C17—H17A0.9600C40—C411.590 (9)
C17—H17B0.9600C40—H40A0.9700
C17—H17C0.9600C40—H40B0.9700
C18—C191.454 (6)C40—H40C0.9700
C18—N51.556 (5)C40—H40D0.9700
C18—H18A0.9700C41—C421.471 (10)
C18—H18B0.9700C41—H41A0.9700
C19—C201.560 (7)C41—H41B0.9700
C19—C20'1.587 (10)C42—H42A0.9600
C19—H19A0.9700C42—H42B0.9600
C19—H19B0.9700C42—H42C0.9600
C19—H19C0.9700C20'—C21'1.525 (10)
C19—H19D0.9700C20'—H20C0.9700
C20—C211.486 (8)C20'—H20D0.9700
C20—H20A0.9700C21'—H21D0.9600
C20—H20B0.9700C21'—H21E0.9600
C21—H21A0.9600C21'—H21F0.9600
C21—H21B0.9600C41'—C42'1.499 (10)
C21—H21C0.9600C41'—H41C0.9700
C22—C231.373 (4)C41'—H41D0.9700
C22—C271.377 (5)C42'—H42D0.9600
C22—N61.432 (4)C42'—H42E0.9600
C23—C241.387 (5)C42'—H42F0.9600
C23—H230.9300N1—N21.384 (4)
C24—C251.372 (5)N2—N31.298 (4)
C24—H240.9300N6—N71.379 (3)
C25—C261.361 (5)N7—N81.292 (4)
C6—C1—C2119.8 (4)N8—C29—C30129.9 (3)
C6—C1—N1121.5 (3)O3—C30—C29129.1 (4)
C2—C1—N1118.8 (3)O3—C30—N10120.7 (4)
C3—C2—C1119.6 (4)C29—C30—N10110.2 (3)
C3—C2—H2120.2N9—C31—O4120.8 (3)
C1—C2—H2120.2N9—C31—N10127.0 (3)
C4—C3—C2121.2 (4)O4—C31—N10112.2 (3)
C4—C3—H3119.4C37—C32—C33120.5 (3)
C2—C3—H3119.4C37—C32—O4117.0 (3)
C3—C4—C5119.4 (4)C33—C32—O4122.0 (3)
C3—C4—H4120.3C34—C33—C32119.3 (3)
C5—C4—H4120.3C34—C33—H33120.3
C4—C5—C6119.9 (4)C32—C33—H33120.3
C4—C5—H5120.1C33—C34—C35121.0 (3)
C6—C5—H5120.1C33—C34—H34119.5
C1—C6—C5120.1 (3)C35—C34—H34119.5
C1—C6—H6119.9O6—C35—C36124.8 (3)
C5—C6—H6119.9O6—C35—C34116.4 (3)
C8—C7—N4127.8 (3)C36—C35—C34118.8 (3)
C8—C7—N1105.1 (3)C35—C36—C37120.5 (3)
N4—C7—N1127.0 (3)C35—C36—H36119.7
C7—C8—N3110.2 (3)C37—C36—H36119.7
C7—C8—C9120.2 (3)C32—C37—C36119.8 (3)
N3—C8—C9129.5 (3)C32—C37—H37120.1
O1—C9—N5120.9 (4)C36—C37—H37120.1
O1—C9—C8128.0 (4)O6—C38—H38A109.5
N5—C9—C8111.0 (3)O6—C38—H38B109.5
N4—C10—O2121.5 (3)H38A—C38—H38B109.5
N4—C10—N5127.2 (3)O6—C38—H38C109.5
O2—C10—N5111.3 (3)H38A—C38—H38C109.5
C12—C11—C16121.4 (3)H38B—C38—H38C109.5
C12—C11—O2116.8 (3)C40—C39—N10109.1 (4)
C16—C11—O2121.2 (3)C40—C39—H39A109.9
C11—C12—C13120.2 (3)N10—C39—H39A109.9
C11—C12—H12119.9C40—C39—H39B109.9
C13—C12—H12119.9N10—C39—H39B109.9
C12—C13—C14119.3 (3)H39A—C39—H39B108.3
C12—C13—H13120.3C39—C40—C41'97.0 (6)
C14—C13—H13120.3C39—C40—C41129.1 (7)
O5—C14—C15115.7 (3)C41'—C40—C4133.0 (6)
O5—C14—C13124.6 (3)C39—C40—H40A105.0
C15—C14—C13119.7 (3)C41'—C40—H40A112.3
C14—C15—C16121.0 (3)C41—C40—H40A105.0
C14—C15—H15119.5C39—C40—H40B105.0
C16—C15—H15119.5C41'—C40—H40B128.6
C11—C16—C15118.3 (3)C41—C40—H40B105.0
C11—C16—H16120.9H40A—C40—H40B105.9
C15—C16—H16120.9C39—C40—H40C111.7
O5—C17—H17A109.5C41'—C40—H40C112.5
O5—C17—H17B109.5C41—C40—H40C101.3
H17A—C17—H17B109.5H40A—C40—H40C7.0
O5—C17—H17C109.5H40B—C40—H40C101.4
H17A—C17—H17C109.5C39—C40—H40D112.6
H17B—C17—H17C109.5C41'—C40—H40D112.7
C19—C18—N5109.9 (4)C41—C40—H40D89.7
C19—C18—H18A109.7H40A—C40—H40D115.4
N5—C18—H18A109.7H40B—C40—H40D16.0
C19—C18—H18B109.7H40C—C40—H40D109.8
N5—C18—H18B109.7C42—C41—C40107.2 (9)
H18A—C18—H18B108.2C42—C41—H41A110.3
C18—C19—C20114.6 (6)C40—C41—H41A110.3
C18—C19—C20'89.4 (7)C42—C41—H41B110.3
C20—C19—C20'28.8 (6)C40—C41—H41B110.3
C18—C19—H19A108.6H41A—C41—H41B108.5
C20—C19—H19A108.6C21'—C20'—C19105.0 (9)
C20'—C19—H19A106.6C21'—C20'—H20C110.7
C18—C19—H19B108.6C19—C20'—H20C110.7
C20—C19—H19B108.6C21'—C20'—H20D110.7
C20'—C19—H19B133.2C19—C20'—H20D110.7
H19A—C19—H19B107.6H20C—C20'—H20D108.8
C18—C19—H19C113.7C20'—C21'—H21D109.5
C20—C19—H19C111.4C20'—C21'—H21E109.5
C20'—C19—H19C113.5H21D—C21'—H21E109.5
H19A—C19—H19C9.2C20'—C21'—H21F109.5
H19B—C19—H19C98.5H21D—C21'—H21F109.5
C18—C19—H19D113.7H21E—C21'—H21F109.5
C20—C19—H19D90.2C42'—C41'—C40105.5 (8)
C20'—C19—H19D114.1C42'—C41'—H41C110.6
H19A—C19—H19D120.1C40—C41'—H41C110.6
H19B—C19—H19D19.2C42'—C41'—H41D110.6
H19C—C19—H19D111.0C40—C41'—H41D110.6
C21—C20—C19107.0 (6)H41C—C41'—H41D108.8
C21—C20—H20A110.3C41'—C42'—H42D109.5
C19—C20—H20A110.3C41'—C42'—H42E109.5
C21—C20—H20B110.3H42D—C42'—H42E109.5
C19—C20—H20B110.3C41'—C42'—H42F109.5
H20A—C20—H20B108.6H42D—C42'—H42F109.5
C23—C22—C27119.8 (3)H42E—C42'—H42F109.5
C23—C22—N6120.9 (3)C7—N1—N2108.1 (3)
C27—C22—N6119.3 (3)C7—N1—C1132.5 (3)
C22—C23—C24119.0 (3)N2—N1—C1119.4 (3)
C22—C23—H23120.5N3—N2—N1108.7 (3)
C24—C23—H23120.5N2—N3—C8107.8 (3)
C25—C24—C23121.0 (3)C10—N4—C7111.3 (3)
C25—C24—H24119.5C10—N5—C9122.4 (3)
C23—C24—H24119.5C10—N5—C18120.5 (3)
C26—C25—C24118.9 (3)C9—N5—C18116.7 (3)
C26—C25—H25120.5C28—N6—N7108.7 (2)
C24—C25—H25120.5C28—N6—C22131.7 (2)
C25—C26—C27121.2 (4)N7—N6—C22119.5 (3)
C25—C26—H26119.4N8—N7—N6108.7 (3)
C27—C26—H26119.4N7—N8—C29108.0 (2)
C26—C27—C22120.1 (3)C31—N9—C28111.8 (2)
C26—C27—H27119.9C31—N10—C30122.8 (3)
C22—C27—H27119.9C31—N10—C39120.7 (3)
N6—C28—N9127.6 (2)C30—N10—C39116.3 (3)
N6—C28—C29105.3 (3)C10—O2—C11121.3 (2)
N9—C28—C29127.0 (3)C31—O4—C32120.4 (2)
C28—C29—N8109.2 (3)C14—O5—C17118.2 (3)
C28—C29—C30121.0 (3)C35—O6—C38117.6 (3)
C6—C1—C2—C3−0.7 (5)N4—C7—N1—N2179.2 (3)
N1—C1—C2—C3178.0 (3)C8—C7—N1—C1−178.7 (3)
C1—C2—C3—C41.1 (6)N4—C7—N1—C10.4 (5)
C2—C3—C4—C5−1.2 (6)C6—C1—N1—C7−13.3 (5)
C3—C4—C5—C60.8 (6)C2—C1—N1—C7168.0 (3)
C2—C1—C6—C50.3 (5)C6—C1—N1—N2168.0 (3)
N1—C1—C6—C5−178.3 (3)C2—C1—N1—N2−10.6 (4)
C4—C5—C6—C1−0.4 (5)C7—N1—N2—N30.2 (3)
N4—C7—C8—N3−179.4 (3)C1—N1—N2—N3179.1 (3)
N1—C7—C8—N3−0.3 (3)N1—N2—N3—C8−0.4 (4)
N4—C7—C8—C9−0.8 (5)C7—C8—N3—N20.4 (4)
N1—C7—C8—C9178.3 (3)C9—C8—N3—N2−178.0 (3)
C7—C8—C9—O1−178.8 (3)O2—C10—N4—C7178.2 (3)
N3—C8—C9—O1−0.5 (6)N5—C10—N4—C7−0.2 (4)
C7—C8—C9—N50.2 (4)C8—C7—N4—C100.8 (4)
N3—C8—C9—N5178.5 (3)N1—C7—N4—C10−178.1 (3)
C16—C11—C12—C131.6 (5)N4—C10—N5—C9−0.4 (5)
O2—C11—C12—C13−170.2 (3)O2—C10—N5—C9−178.9 (3)
C11—C12—C13—C14−0.2 (4)N4—C10—N5—C18172.7 (3)
C12—C13—C14—O5179.2 (3)O2—C10—N5—C18−5.9 (5)
C12—C13—C14—C15−1.7 (5)O1—C9—N5—C10179.4 (3)
O5—C14—C15—C16−178.5 (3)C8—C9—N5—C100.3 (5)
C13—C14—C15—C162.3 (5)O1—C9—N5—C186.1 (5)
C12—C11—C16—C15−1.0 (5)C8—C9—N5—C18−173.0 (3)
O2—C11—C16—C15170.4 (3)C19—C18—N5—C1096.9 (4)
C14—C15—C16—C11−1.0 (5)C19—C18—N5—C9−89.7 (4)
N5—C18—C19—C20−175.0 (4)N9—C28—N6—N7−178.9 (2)
N5—C18—C19—C20'170.7 (10)C29—C28—N6—N7−0.1 (3)
C18—C19—C20—C21−72.3 (10)N9—C28—N6—C22−0.8 (4)
C20'—C19—C20—C21−41 (2)C29—C28—N6—C22178.0 (2)
C27—C22—C23—C240.9 (4)C23—C22—N6—C2810.2 (4)
N6—C22—C23—C24−179.4 (3)C27—C22—N6—C28−170.0 (3)
C22—C23—C24—C25−0.4 (5)C23—C22—N6—N7−171.8 (2)
C23—C24—C25—C26−0.3 (5)C27—C22—N6—N77.9 (4)
C24—C25—C26—C270.5 (6)C28—N6—N7—N80.1 (3)
C25—C26—C27—C22−0.1 (6)C22—N6—N7—N8−178.3 (2)
C23—C22—C27—C26−0.7 (5)N6—N7—N8—C290.0 (3)
N6—C22—C27—C26179.6 (3)C28—C29—N8—N7−0.1 (3)
N6—C28—C29—N80.1 (3)C30—C29—N8—N7−179.2 (3)
N9—C28—C29—N8178.9 (2)O4—C31—N9—C28−177.3 (3)
N6—C28—C29—C30179.3 (3)N10—C31—N9—C281.1 (4)
N9—C28—C29—C30−1.9 (4)N6—C28—N9—C31−179.1 (3)
C28—C29—C30—O3177.9 (3)C29—C28—N9—C312.4 (4)
N8—C29—C30—O3−3.1 (6)N9—C31—N10—C30−5.1 (5)
C28—C29—C30—N10−1.8 (4)O4—C31—N10—C30173.4 (3)
N8—C29—C30—N10177.2 (3)N9—C31—N10—C39169.6 (4)
C37—C32—C33—C341.7 (5)O4—C31—N10—C39−11.9 (5)
O4—C32—C33—C34−170.3 (3)O3—C30—N10—C31−174.8 (3)
C32—C33—C34—C350.9 (5)C29—C30—N10—C315.0 (4)
C33—C34—C35—O6176.0 (3)O3—C30—N10—C3910.3 (5)
C33—C34—C35—C36−2.8 (5)C29—C30—N10—C39−169.9 (4)
O6—C35—C36—C37−176.5 (3)C40—C39—N10—C3191.3 (5)
C34—C35—C36—C372.3 (5)C40—C39—N10—C30−93.7 (5)
C33—C32—C37—C36−2.2 (5)N4—C10—O2—C118.4 (5)
O4—C32—C37—C36170.1 (3)N5—C10—O2—C11−173.0 (3)
C35—C36—C37—C320.2 (5)C12—C11—O2—C10−132.0 (3)
N10—C39—C40—C41'170.7 (7)C16—C11—O2—C1056.2 (4)
N10—C39—C40—C41179.6 (11)N9—C31—O4—C32−7.8 (5)
C39—C40—C41—C42−25 (2)N10—C31—O4—C32173.6 (3)
C41'—C40—C41—C42−9.0 (16)C37—C32—O4—C31128.2 (3)
C18—C19—C20'—C21'174.3 (17)C33—C32—O4—C31−59.6 (4)
C20—C19—C20'—C21'22.1 (13)C15—C14—O5—C17166.1 (3)
C39—C40—C41'—C42'−177.3 (11)C13—C14—O5—C17−14.8 (5)
C41—C40—C41'—C42'15.4 (17)C36—C35—O6—C3811.9 (5)
C8—C7—N1—N20.1 (3)C34—C35—O6—C38−166.9 (4)
  9 in total

1.  Guanase activity in normal and neoplastic human tissue.

Authors:  R LEVINE; T C HALL; C A HARRIS
Journal:  Cancer       Date:  1963-02       Impact factor: 6.860

2.  A short history of SHELX.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr A       Date:  2007-12-21       Impact factor: 2.290

3.  Experimental evaluation of potential anticancer agents. IX. The ribonucleosides and ribonucleotides of two purine antagonists.

Authors:  J A MONTGOMERY; F M SCHABEL; H E SKIPPER
Journal:  Cancer Res       Date:  1962-05       Impact factor: 12.701

4.  Antiviral agents. 2. Structure-activity relationships of compounds related to 1-adamantanamine.

Authors:  P E Aldrich; E C Hermann; W E Meier; M Paulshock; W W Prichard; J A Snyder; J C Watts
Journal:  J Med Chem       Date:  1971-06       Impact factor: 7.446

5.  8-azatheophylline and its derivatives as coronary vasodilators.

Authors:  D S Bariana
Journal:  J Med Chem       Date:  1971-06       Impact factor: 7.446

6.  Inhibitory effect of 8-azuguanine on the development of tolerance in the analgesic action of morphine.

Authors:  I Yamamoto; R Inoki; Y Tamari; K Iwatsubo
Journal:  Jpn J Pharmacol       Date:  1967-03

7.  5-(4-Chloro-phen-oxy)-6-isopropyl-3-phenyl-3H-1,2,3-triazolo[4,5-d]pyrimidin-7(6H)-one.

Authors:  Xiao-Hua Zeng; Xiao-Ling Liu; Shou-Heng Deng; Ping Chen; Hong-Mei Wang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-09-30

8.  Application of bis(iminophosphorane) in heterocyclic synthesis: new entries to symmetrically or unsymmetrically substituted thieno[2,3-d:5,4-d']dipyrimidine-4,5(3H,6H)-diones.

Authors:  Ming-Wu Ding; Sheng-Zhen Xu; Jun-Feng Zhao
Journal:  J Org Chem       Date:  2004-11-26       Impact factor: 4.354

9.  Structure validation in chemical crystallography.

Authors:  Anthony L Spek
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2009-01-20
  9 in total

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