5-Bromopyridine-2,3-diamine → HCID 178478348, compound

HRID 2218341Notes

Reaction equation

HRID 2218341 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH2:9])[C:5]([NH2:8])=[N:6][CH:7]=1.[Cl:10][C:11]1[S:12][C:13]([CH2:16][O:17][C:18]2[CH:25]=[CH:24][C:21]([CH:22]=O)=[CH:20][CH:19]=2)=[CH:14][N:15]=1>>[Br:1][C:2]1[CH:3]=[C:4]2[N:9]=[C:22]([C:21]3[CH:20]=[CH:19][C:18]([O:17][CH2:16][C:13]4[S:12][C:11]([Cl:10])=[N:15][CH:14]=4)=[CH:25][CH:24]=3)[NH:8][C:5]2=[N:6][CH:7]=1

Participants

3

Reactant 2

HCID 6911565-Bromopyridine-2,3-diamineHCID 27635264-[(2-chloro-1,3-thiazol-5-yl)methoxy]benzaldehyde

Product 1

HCID 178478348HCID 178478348, compound

Procedure

The title compound was prepared from 5-bromo-2,3-diaminopyridine and 4-[(2-chloro-1,3-thiazol-5-yl)methoxy]benzaldehyde.

Sources & evidence

ORD record
ord-731a64e0963540ab896aa3bc2524525e
Source dataset
uspto-grants-2008_08
Patent number
US07410966B2

Reaction notes

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