2-Bromo-4-methylpyridine → HCID 67428946, compound

HRID 1661287Notes

Reaction equation

HRID 1661287 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[C:22]([F:23])=[CH:21][CH:20]=[CH:19][C:18]=3[O:24][CH3:25])[CH:14]=[CH:15][CH:16]=2)[CH:10]=1)=[O:5].Br[C:28]1[CH:33]=[C:32]([CH3:34])[CH:31]=[CH:30][N:29]=1>>[F:23][C:22]1[C:17]([C:13]2[CH:14]=[CH:15][CH:16]=[C:11]([N:9]3[CH:10]=[C:6]([C:4]([C:28]4[CH:33]=[C:32]([CH3:34])[CH:31]=[CH:30][N:29]=4)=[O:5])[N:7]=[CH:8]3)[CH:12]=2)=[C:18]([O:24][CH3:25])[CH:19]=[CH:20][CH:21]=1

Participants

3

Reactant 2

HCID 27340872-Bromo-4-methylpyridineHCID 87396699HCID 87396699, compound

Product 1

HCID 67428946HCID 67428946, compound

Procedure

This compound is prepared by method C using compound 12g and 2-bromo-4-methylpyridine

Workup

  1. customThis compound is prepared by method C

Sources & evidence

ORD record
ord-3356d47bf9574813af3fe7686ed08cc1
Source dataset
uspto-grants-2011_10
Patent number
US08030339B2

Reaction notes

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