4-[3-(Dimethylamino)propoxy]benzaldehyde → HCID 178483565, compound

HRID 2218340Notes

Reaction equation

HRID 2218340 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH2:9])[C:5]([NH2:8])=[N:6][CH:7]=1.[CH3:10][N:11]([CH3:24])[CH2:12][CH2:13][CH2:14][O:15][C:16]1[CH:23]=[CH:22][C:19]([CH:20]=O)=[CH:18][CH:17]=1>>[Br:1][C:2]1[CH:3]=[C:4]2[N:9]=[C:20]([C:19]3[CH:22]=[CH:23][C:16]([O:15][CH2:14][CH2:13][CH2:12][N:11]([CH3:24])[CH3:10])=[CH:17][CH:18]=3)[NH:8][C:5]2=[N:6][CH:7]=1

Participants

3

Reactant 2

HCID 5469324-[3-(Dimethylamino)propoxy]benzaldehydeHCID 6911565-Bromopyridine-2,3-diamine

Product 1

HCID 178483565HCID 178483565, compound

Procedure

The title compound was prepared from 5-bromo-2,3-diaminopyridine (376 mg, 2 mmol) and 4-[3-(dimethylamino)-propoxy]benzaldehyde (420 mg, 2 mmol).

Sources & evidence

ORD record
ord-610e693ba28f4aa7a1c5eec466af60e9
Source dataset
uspto-grants-2008_08
Patent number
US07410966B2

Reaction notes

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