Benzaldehyde → HCID 178419436, compound

HRID 2218377Notes

Reaction equation

HRID 2218377 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:9]([C:11]3[CH:17]=[CH:16][C:14]([NH2:15])=[CH:13][CH:12]=3)[NH:8][C:5]2=[N:6][CH:7]=1.[CH:18](=O)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[CH2:18]([NH:15][C:14]1[CH:16]=[CH:17][C:11]([C:9]2[NH:8][C:5]3=[N:6][CH:7]=[C:2]([Br:1])[CH:3]=[C:4]3[N:10]=2)=[CH:12][CH:13]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 240BenzaldehydeHCID 178507423HCID 178507423, compound

Product 1

HCID 178419436HCID 178419436, compound

Procedure

The title compound was prepared from 4-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)aniline (0.289 g, 1 mmol) and benzaldehyde (0.106 g, 1 mmol).

Sources & evidence

ORD record
ord-af1a7075edfb43348e43502e5f439964
Source dataset
uspto-grants-2008_08
Patent number
US07410966B2

Reaction notes

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