HCID 22387825, compound → 3H-Imidazo[4,5-b]pyridine-5-carbonitrile, 2-methyl-

HRID 1699816Notes

Reaction equation

HRID 1699816 reaction equation
ClC1C=C(C2C=CC=CC=2)C=CC=1C[N:5]1[C:9]2=[N:10][C:11]([C:14]#[N:15])=[CH:12][CH:13]=[C:8]2[N:7]=[C:6]1[CH3:16].ClC1C=C(C2C=CC=CC=2)C=CC=1CN1C2C(=NC(C#N)=CC=2)N=C1C>>[CH3:16][C:6]1[NH:7][C:8]2[C:9]([N:5]=1)=[N:10][C:11]([C:14]#[N:15])=[CH:12][CH:13]=2

Participants

3

Reactant 2

HCID 22387825HCID 22387825, compoundHCID 22388245HCID 22388245, compound

Product 1

HCID 223881363H-Imidazo[4,5-b]pyridine-5-carbonitrile, 2-methyl-

Procedure

In the same manner as in the following Preparation Example 14-2, 3-(2-chloro-4-phenylbenzyl)-2-methyl-3H-imidazo[4,5-b]pyridine-5-carbonitrile (163 mg and 1-(2-chloro-4-phenylbenzyl)-2-methyl-1H-imidazo-[4,5-b]pyridine-5-carbonitrile (113 mg) were respectively obtained as pale-yellow crystals and pale-yellow amorphous from 2-methyl-1H-imidazo[4,5-b]pyridine-5-carbonitrile (200 mg).

Sources & evidence

ORD record
ord-c0d2663793e140329f32065cc0689a58
Source dataset
uspto-grants-2002_02
Patent number
US06348474B1

Reaction notes

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