2-Bromo-3-methylpyridine → HCID 16679107, compound

HRID 1661273Notes

Reaction equation

HRID 1661273 reaction equation
CON(C)[C:4]([C:6]1[N:7]=[CH:8][N:9]([C:11]2[CH:12]=[C:13]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[O:23][C:24]([F:27])([F:26])[F:25])[CH:14]=[CH:15][CH:16]=2)[CH:10]=1)=[O:5].Br[C:30]1[C:35]([CH3:36])=[CH:34][CH:33]=[CH:32][N:31]=1>>[CH3:36][C:35]1[C:30]([C:4]([C:6]2[N:7]=[CH:8][N:9]([C:11]3[CH:12]=[C:13]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=4[O:23][C:24]([F:25])([F:27])[F:26])[CH:14]=[CH:15][CH:16]=3)[CH:10]=2)=[O:5])=[N:31][CH:32]=[CH:33][CH:34]=1

Participants

3

Procedure

This compound is prepared by method C using compound 12f and 2-bromo-3-methylpyridine

Workup

  1. customThis compound is prepared by method C

Sources & evidence

ORD record
ord-b676c9862f09443b8064428f879e1e75
Source dataset
uspto-grants-2011_10
Patent number
US08030339B2

Reaction notes

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