3-Methyl-5-phenyl-1-(3-phenyl-isoquinolin-1-yl)-1H-pyrazole.

The title compound, C(25)H(19)N(3), is composed of an aryl-substituted pyrazole ring connected to an aryl-substituted isoquinoline ring system with a dihedral angle of 52.7 (1)° between the pyrazole ring and the isoquinoline ring system. The dihedral angle between the pyrazole ring and the phenyl ring attached to it is 27.4 (1)° and the dihedral angle between the isoquinoline ring system and the phenyl ring attached to it is 19.6 (1)°.

Related literature

For medicinal applications of hydrazine derivatives, see: Broadhurst et al. (2001 ▶).

Experimental

Crystal data

C25H19N3

M = 361.43

Orthorhombic,

a = 10.9610 (9) Å

b = 16.8078 (13) Å

c = 21.3118 (17) Å

V = 3926.3 (5) Å3

Z = 8

Mo Kα radiation

μ = 0.07 mm−1

T = 290 K

0.42 × 0.23 × 0.20 mm

Data collection

Bruker SMART area-detector diffractometer

26302 measured reflections

3452 independent reflections

2031 reflections with I > 2σ(I)

R int = 0.091

Refinement

R[F 2 > 2σ(F 2)] = 0.059

wR(F 2) = 0.172

S = 1.04

3452 reflections

254 parameters

H-atom parameters constrained

Δρmax = 0.16 e Å−3

Δρmin = −0.16 e Å−3

Data collection: SMART (Bruker, 2004 ▶); cell refinement: SAINT (Bruker, 2004 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: X-SEED (Barbour, 2001 ▶); software used to prepare material for publication: publCIF (Westrip, 2010 ▶).

Crystal structure: contains datablocks global, I. DOI: 10.1107/S160053680905572X/bt5159sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S160053680905572X/bt5159Isup2.hkl

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

C25H19N3	F(000) = 1520
Mr = 361.43	Dx = 1.223 Mg m−3
Orthorhombic, Pbca	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ac 2ab	Cell parameters from 1667 reflections
a = 10.9610 (9) Å	θ = 2.4–19.5°
b = 16.8078 (13) Å	µ = 0.07 mm−1
c = 21.3118 (17) Å	T = 290 K
V = 3926.3 (5) Å3	Block, colorless
Z = 8	0.42 × 0.23 × 0.20 mm

Bruker SMART area-detector diffractometer	2031 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tube	Rint = 0.091
graphite	θmax = 25.0°, θmin = 1.9°
φ and ω scans	h = −13→13
26302 measured reflections	k = −19→19
3452 independent reflections	l = −25→25

Refinement on F2	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.059	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.172	H-atom parameters constrained
S = 1.04	w = 1/[σ2(Fo2) + (0.0822P)2 + 0.3609P] where P = (Fo2 + 2Fc2)/3
3452 reflections	(Δ/σ)max = 0.001
254 parameters	Δρmax = 0.16 e Å−3
0 restraints	Δρmin = −0.16 e Å−3

	x	y	z	Uiso*/Ueq
N1	0.42399 (17)	0.56804 (11)	0.65341 (8)	0.0632 (5)
N2	0.58627 (17)	0.61748 (12)	0.59624 (9)	0.0707 (6)
N3	0.70861 (18)	0.60123 (14)	0.60212 (10)	0.0846 (7)
C1	0.5164 (2)	0.61722 (15)	0.65309 (11)	0.0634 (6)
C2	0.5528 (2)	0.66672 (14)	0.70362 (11)	0.0633 (6)
C3	0.6493 (2)	0.72259 (17)	0.70207 (14)	0.0799 (8)
H3	0.6940	0.7293	0.6654	0.096*
C4	0.6771 (3)	0.76627 (17)	0.75330 (18)	0.0925 (9)
H4	0.7414	0.8023	0.7517	0.111*
C5	0.6101 (3)	0.75780 (18)	0.80879 (16)	0.0963 (9)
H5	0.6304	0.7881	0.8438	0.116*
C6	0.5156 (3)	0.70560 (18)	0.81196 (14)	0.0876 (8)
H6	0.4713	0.7006	0.8490	0.105*
C7	0.4844 (2)	0.65902 (14)	0.75938 (11)	0.0681 (6)
C8	0.3851 (2)	0.60570 (14)	0.75944 (11)	0.0691 (7)
H8	0.3392	0.5993	0.7958	0.083*
C9	0.3554 (2)	0.56334 (14)	0.70713 (11)	0.0617 (6)
C10	0.2482 (2)	0.50980 (14)	0.70392 (11)	0.0635 (6)
C11	0.1918 (2)	0.48178 (15)	0.75749 (12)	0.0745 (7)
H11	0.2226	0.4958	0.7966	0.089*
C12	0.0904 (3)	0.43317 (16)	0.75384 (15)	0.0858 (8)
H12	0.0538	0.4149	0.7905	0.103*
C13	0.0441 (3)	0.4121 (2)	0.69771 (17)	0.0999 (10)
H13	−0.0241	0.3793	0.6955	0.120*
C14	0.0978 (3)	0.4392 (2)	0.64406 (16)	0.1194 (12)
H14	0.0660	0.4248	0.6052	0.143*
C15	0.1993 (3)	0.4880 (2)	0.64698 (13)	0.0944 (9)
H15	0.2350	0.5062	0.6101	0.113*
C16	0.8797 (3)	0.5726 (3)	0.53211 (16)	0.1305 (13)
H16A	0.9202	0.5639	0.5715	0.196*
H16B	0.9171	0.6166	0.5108	0.196*
H16C	0.8864	0.5257	0.5067	0.196*
C17	0.7463 (2)	0.59087 (19)	0.54383 (14)	0.0888 (8)
C18	0.6524 (3)	0.59926 (17)	0.50078 (13)	0.0849 (8)
H18	0.6579	0.5946	0.4574	0.102*
C19	0.5500 (2)	0.61580 (14)	0.53516 (12)	0.0688 (7)
C20	0.4262 (2)	0.63444 (15)	0.51195 (12)	0.0700 (7)
C21	0.3472 (3)	0.68436 (17)	0.54353 (13)	0.0869 (8)
H21	0.3704	0.7068	0.5816	0.104*
C22	0.2326 (3)	0.7011 (2)	0.51841 (16)	0.1031 (10)
H22	0.1792	0.7335	0.5407	0.124*
C23	0.1976 (3)	0.6712 (2)	0.46237 (18)	0.1081 (10)
H23	0.1214	0.6835	0.4458	0.130*
C24	0.2752 (3)	0.6231 (2)	0.43068 (16)	0.1117 (11)
H24	0.2522	0.6027	0.3919	0.134*
C25	0.3885 (3)	0.60395 (18)	0.45521 (13)	0.0887 (8)
H25	0.4398	0.5700	0.4330	0.106*

	U11	U22	U33	U12	U13	U23
N1	0.0544 (11)	0.0749 (13)	0.0603 (12)	0.0075 (10)	0.0015 (10)	0.0039 (9)
N2	0.0542 (12)	0.0933 (15)	0.0646 (13)	0.0066 (11)	0.0042 (10)	0.0105 (10)
N3	0.0552 (13)	0.1212 (19)	0.0773 (15)	0.0096 (12)	0.0066 (11)	0.0139 (13)
C1	0.0534 (13)	0.0770 (16)	0.0598 (15)	0.0118 (13)	0.0008 (11)	0.0094 (12)
C2	0.0553 (14)	0.0668 (15)	0.0679 (16)	0.0089 (12)	−0.0046 (12)	0.0053 (12)
C3	0.0663 (16)	0.0801 (18)	0.093 (2)	0.0056 (15)	−0.0055 (14)	0.0093 (15)
C4	0.0795 (19)	0.0796 (19)	0.118 (3)	−0.0061 (15)	−0.0244 (19)	0.0043 (19)
C5	0.100 (2)	0.090 (2)	0.099 (3)	0.0029 (19)	−0.0241 (19)	−0.0117 (17)
C6	0.091 (2)	0.091 (2)	0.081 (2)	0.0016 (18)	−0.0062 (15)	−0.0128 (15)
C7	0.0642 (14)	0.0718 (15)	0.0682 (17)	0.0086 (13)	−0.0041 (13)	−0.0033 (13)
C8	0.0652 (15)	0.0802 (17)	0.0619 (16)	0.0128 (13)	0.0063 (12)	−0.0027 (13)
C9	0.0550 (13)	0.0701 (15)	0.0600 (15)	0.0128 (12)	0.0043 (11)	0.0010 (12)
C10	0.0557 (13)	0.0697 (15)	0.0652 (16)	0.0103 (12)	0.0054 (12)	−0.0026 (12)
C11	0.0721 (16)	0.0797 (17)	0.0717 (17)	0.0030 (14)	0.0063 (14)	0.0030 (13)
C12	0.0782 (18)	0.0835 (18)	0.096 (2)	0.0000 (15)	0.0207 (17)	0.0067 (16)
C13	0.076 (2)	0.113 (2)	0.110 (3)	−0.0224 (17)	0.0062 (18)	−0.002 (2)
C14	0.102 (2)	0.164 (3)	0.092 (2)	−0.051 (2)	−0.0043 (19)	−0.012 (2)
C15	0.0830 (18)	0.129 (3)	0.0713 (18)	−0.0221 (18)	0.0066 (15)	−0.0034 (17)
C16	0.0710 (19)	0.202 (4)	0.119 (3)	0.025 (2)	0.0287 (18)	0.014 (3)
C17	0.0685 (17)	0.121 (2)	0.0765 (19)	0.0118 (16)	0.0171 (15)	0.0141 (17)
C18	0.0853 (19)	0.106 (2)	0.0633 (16)	0.0106 (16)	0.0141 (15)	0.0110 (14)
C19	0.0733 (16)	0.0701 (16)	0.0630 (16)	0.0038 (13)	0.0045 (13)	0.0093 (12)
C20	0.0748 (16)	0.0685 (15)	0.0667 (17)	0.0027 (13)	0.0002 (14)	0.0110 (12)
C21	0.091 (2)	0.093 (2)	0.0768 (18)	0.0228 (17)	−0.0073 (15)	0.0028 (14)
C22	0.097 (2)	0.121 (3)	0.091 (2)	0.0377 (19)	−0.0039 (19)	0.0170 (18)
C23	0.084 (2)	0.144 (3)	0.097 (3)	0.017 (2)	−0.0086 (19)	0.022 (2)
C24	0.101 (2)	0.145 (3)	0.089 (2)	−0.005 (2)	−0.024 (2)	−0.004 (2)
C25	0.089 (2)	0.102 (2)	0.0748 (19)	0.0065 (17)	−0.0030 (16)	−0.0044 (15)

N1—C1	1.308 (3)	C12—H12	0.9300
N1—C9	1.372 (3)	C13—C14	1.365 (4)
N2—C19	1.362 (3)	C13—H13	0.9300
N2—N3	1.374 (3)	C14—C15	1.383 (4)
N2—C1	1.433 (3)	C14—H14	0.9300
N3—C17	1.321 (3)	C15—H15	0.9300
C1—C2	1.418 (3)	C16—C17	1.515 (4)
C2—C7	1.411 (3)	C16—H16A	0.9600
C2—C3	1.414 (3)	C16—H16B	0.9600
C3—C4	1.351 (4)	C16—H16C	0.9600
C3—H3	0.9300	C17—C18	1.385 (4)
C4—C5	1.399 (4)	C18—C19	1.370 (3)
C4—H4	0.9300	C18—H18	0.9300
C5—C6	1.359 (4)	C19—C20	1.478 (3)
C5—H5	0.9300	C20—C25	1.377 (3)
C6—C7	1.409 (3)	C20—C21	1.381 (4)
C6—H6	0.9300	C21—C22	1.394 (4)
C7—C8	1.410 (3)	C21—H21	0.9300
C8—C9	1.362 (3)	C22—C23	1.351 (4)
C8—H8	0.9300	C22—H22	0.9300
C9—C10	1.481 (3)	C23—C24	1.355 (5)
C10—C15	1.376 (3)	C23—H23	0.9300
C10—C11	1.381 (3)	C24—C25	1.385 (4)
C11—C12	1.382 (4)	C24—H24	0.9300
C11—H11	0.9300	C25—H25	0.9300
C12—C13	1.347 (4)
C1—N1—C9	117.7 (2)	C12—C13—H13	120.2
C19—N2—N3	111.61 (19)	C14—C13—H13	120.2
C19—N2—C1	130.7 (2)	C13—C14—C15	120.5 (3)
N3—N2—C1	116.34 (19)	C13—C14—H14	119.7
C17—N3—N2	104.2 (2)	C15—C14—H14	119.8
N1—C1—C2	125.8 (2)	C10—C15—C14	120.7 (3)
N1—C1—N2	114.9 (2)	C10—C15—H15	119.6
C2—C1—N2	119.3 (2)	C14—C15—H15	119.6
C7—C2—C3	118.5 (2)	C17—C16—H16A	109.5
C7—C2—C1	115.9 (2)	C17—C16—H16B	109.5
C3—C2—C1	125.6 (2)	H16A—C16—H16B	109.5
C4—C3—C2	120.7 (3)	C17—C16—H16C	109.5
C4—C3—H3	119.6	H16A—C16—H16C	109.5
C2—C3—H3	119.6	H16B—C16—H16C	109.5
C3—C4—C5	120.6 (3)	N3—C17—C18	112.2 (2)
C3—C4—H4	119.7	N3—C17—C16	118.9 (3)
C5—C4—H4	119.7	C18—C17—C16	128.9 (3)
C6—C5—C4	120.5 (3)	C19—C18—C17	106.0 (2)
C6—C5—H5	119.7	C19—C18—H18	127.0
C4—C5—H5	119.7	C17—C18—H18	127.0
C5—C6—C7	120.3 (3)	N2—C19—C18	106.0 (2)
C5—C6—H6	119.9	N2—C19—C20	125.7 (2)
C7—C6—H6	119.9	C18—C19—C20	128.1 (2)
C8—C7—C2	118.0 (2)	C25—C20—C21	117.8 (3)
C8—C7—C6	122.7 (2)	C25—C20—C19	119.4 (2)
C2—C7—C6	119.3 (2)	C21—C20—C19	122.8 (2)
C9—C8—C7	121.1 (2)	C20—C21—C22	120.0 (3)
C9—C8—H8	119.5	C20—C21—H21	120.0
C7—C8—H8	119.5	C22—C21—H21	120.0
C8—C9—N1	121.5 (2)	C23—C22—C21	121.4 (3)
C8—C9—C10	123.0 (2)	C23—C22—H22	119.3
N1—C9—C10	115.5 (2)	C21—C22—H22	119.3
C15—C10—C11	117.6 (2)	C22—C23—C24	118.9 (3)
C15—C10—C9	120.8 (2)	C22—C23—H23	120.5
C11—C10—C9	121.6 (2)	C24—C23—H23	120.5
C12—C11—C10	121.0 (2)	C23—C24—C25	120.9 (3)
C12—C11—H11	119.5	C23—C24—H24	119.5
C10—C11—H11	119.5	C25—C24—H24	119.5
C13—C12—C11	120.6 (3)	C20—C25—C24	120.9 (3)
C13—C12—H12	119.7	C20—C25—H25	119.5
C11—C12—H12	119.7	C24—C25—H25	119.5
C12—C13—C14	119.6 (3)
C19—N2—N3—C17	0.9 (3)	N1—C9—C10—C11	161.5 (2)
C1—N2—N3—C17	169.0 (2)	C15—C10—C11—C12	0.4 (4)
C9—N1—C1—C2	0.0 (3)	C9—C10—C11—C12	178.7 (2)
C9—N1—C1—N2	178.25 (18)	C10—C11—C12—C13	−0.1 (4)
C19—N2—C1—N1	42.3 (3)	C11—C12—C13—C14	−0.1 (5)
N3—N2—C1—N1	−123.0 (2)	C12—C13—C14—C15	0.1 (5)
C19—N2—C1—C2	−139.3 (2)	C11—C10—C15—C14	−0.4 (4)
N3—N2—C1—C2	55.3 (3)	C9—C10—C15—C14	−178.7 (3)
N1—C1—C2—C7	2.4 (3)	C13—C14—C15—C10	0.2 (5)
N2—C1—C2—C7	−175.80 (18)	N2—N3—C17—C18	−0.5 (3)
N1—C1—C2—C3	−176.8 (2)	N2—N3—C17—C16	179.2 (3)
N2—C1—C2—C3	5.1 (3)	N3—C17—C18—C19	−0.1 (3)
C7—C2—C3—C4	1.6 (3)	C16—C17—C18—C19	−179.8 (3)
C1—C2—C3—C4	−179.3 (2)	N3—N2—C19—C18	−1.0 (3)
C2—C3—C4—C5	−0.8 (4)	C1—N2—C19—C18	−166.9 (2)
C3—C4—C5—C6	−0.2 (4)	N3—N2—C19—C20	−176.8 (2)
C4—C5—C6—C7	0.4 (4)	C1—N2—C19—C20	17.3 (4)
C3—C2—C7—C8	177.2 (2)	C17—C18—C19—N2	0.6 (3)
C1—C2—C7—C8	−2.0 (3)	C17—C18—C19—C20	176.3 (3)
C3—C2—C7—C6	−1.4 (3)	N2—C19—C20—C25	−156.5 (2)
C1—C2—C7—C6	179.4 (2)	C18—C19—C20—C25	28.6 (4)
C5—C6—C7—C8	−178.1 (2)	N2—C19—C20—C21	26.4 (4)
C5—C6—C7—C2	0.4 (4)	C18—C19—C20—C21	−148.5 (3)
C2—C7—C8—C9	−0.5 (3)	C25—C20—C21—C22	1.3 (4)
C6—C7—C8—C9	178.0 (2)	C19—C20—C21—C22	178.5 (2)
C7—C8—C9—N1	3.1 (3)	C20—C21—C22—C23	−2.0 (5)
C7—C8—C9—C10	−176.8 (2)	C21—C22—C23—C24	1.0 (5)
C1—N1—C9—C8	−2.8 (3)	C22—C23—C24—C25	0.6 (6)
C1—N1—C9—C10	177.05 (19)	C21—C20—C25—C24	0.3 (4)
C8—C9—C10—C15	159.6 (2)	C19—C20—C25—C24	−177.0 (3)
N1—C9—C10—C15	−20.2 (3)	C23—C24—C25—C20	−1.2 (5)
C8—C9—C10—C11	−18.6 (3)