5-Bromopyridine-2,3-diamine → HCID 178419443, compound

HRID 2218342Notes

Reaction equation

HRID 2218342 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH2:9])[C:5]([NH2:8])=[N:6][CH:7]=1.[N:10]1([CH2:16][CH2:17][O:18][C:19]2[CH:26]=[CH:25][C:22]([CH:23]=O)=[CH:21][CH:20]=2)[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1>>[Br:1][C:2]1[CH:3]=[C:4]2[N:9]=[C:23]([C:22]3[CH:21]=[CH:20][C:19]([O:18][CH2:17][CH2:16][N:10]4[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]4)=[CH:26][CH:25]=3)[NH:8][C:5]2=[N:6][CH:7]=1

Participants

3

Reactant 2

HCID 6911565-Bromopyridine-2,3-diamineHCID 111838924-(2-(Piperidin-1-yl)ethoxy)benzaldehyde

Product 1

HCID 178419443HCID 178419443, compound

Procedure

The title compound was prepared from 5-bromo-2,3-diaminopyridine and 4-[2-(1-piperidinyl)ethoxy]benzaldehyde.

Sources & evidence

ORD record
ord-0964860117d74ea3ad5b85a70763287c
Source dataset
uspto-grants-2008_08
Patent number
US07410966B2

Reaction notes

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