2-Bromopyridine → HCID 68436114, compound

HRID 1170102Notes

Reaction equation

HRID 1170102 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[CH3:15][C:16]1[O:20][C:19]([CH2:21][NH2:22])=[CH:18][CH:17]=1.Br[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=1>>[CH3:15][C:16]1[O:20][C:19]([CH2:21][NH:22][C:8]2[CH:7]=[CH:6][C:5]3[C:4]([NH:1][C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=4)=[CH:13][CH:12]=[CH:11][C:10]=3[N:9]=2)=[CH:18][CH:17]=1

Participants

4

Reactant 3

HCID 79732-BromopyridineHCID 3192512-Chloro-5-nitroquinolineHCID 27246835-Methyl-2-furylmethylamine

Product 1

HCID 68436114HCID 68436114, compound

Procedure

The title compound, MS: m/e=331.4 (M+H+), was prepared in accordance with the general method of example 38 from 5-nitro-2-chloroquinoline, 5-methyl-2-furanmethanamine and 2-bromopyridine.

Sources & evidence

ORD record
ord-2e152b8dc7f247448b06700bd7fe38fb
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Reaction notes

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