2-Bromo-4-methylpyridine → HCID 16679108, compound

HRID 1661274Notes

Reaction equation

HRID 1661274 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[CH:35]=[C:34]([CH3:36])[CH:33]=[CH:32][N:31]=1>>[CH3:36][C:34]1[CH:33]=[CH:32][N:31]=[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])[CH:35]=1

Participants

3

Reactant 2

HCID 27340872-Bromo-4-methylpyridineHCID 86634432HCID 86634432, compound

Product 1

HCID 16679108HCID 16679108, compound

Procedure

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

Workup

  1. customThis compound is prepared by method C

Sources & evidence

ORD record
ord-3aaf2349f2eb455690f3e000b97404c3
Source dataset
uspto-grants-2011_10
Patent number
US08030339B2

Reaction notes

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