3-Bromopyridine → HCID 68434058, compound

HRID 1170100Notes

Reaction equation

HRID 1170100 reaction equation
[CH3:1][C:2]1[O:6][C:5]([CH2:7][NH:8][C:9]2[CH:18]=[CH:17][C:16]3[C:15]([NH2:19])=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=2)=[CH:4][CH:3]=1.Br[C:21]1[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=1>>[CH3:1][C:2]1[O:6][C:5]([CH2:7][NH:8][C:9]2[CH:18]=[CH:17][C:16]3[C:15]([NH:19][C:21]4[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=4)=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=2)=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 122863-BromopyridineHCID 44217679HCID 44217679, compound

Product 1

HCID 68434058HCID 68434058, compound

Procedure

The title compound, MS: m/e=331.3 (M+H+), was prepared from N2-(5-methyl-furan-2-ylmethyl)-quinoline-2,5-diamine and 3-bromopyridine as described in example 1 step B.

Sources & evidence

ORD record
ord-f1419dba2e734b0189aca82b51287be8
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Reaction notes

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