2-Bromo-4-methylpyridine → HCID 87396729, compound

HRID 1661333Notes

Reaction equation

HRID 1661333 reaction equation
CON(C)[C:4]([C:6]1[N:7]=[CH:8][N:9]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([C:17]3[C:18]([Cl:23])=[N:19][CH:20]=[CH:21][CH:22]=3)[CH:12]=2)[CH:10]=1)=[O:5].Br[C:26]1[CH:31]=[C:30]([CH3:32])[CH:29]=[CH:28][N:27]=1>>[Cl:23][C:18]1[C:17]([C:13]2[CH:12]=[C:11]([N:9]3[CH:10]=[C:6]([C:4]([C:26]4[CH:31]=[C:30]([CH3:32])[CH:29]=[CH:28][N:27]=4)=[O:5])[N:7]=[CH:8]3)[CH:16]=[CH:15][CH:14]=2)=[CH:22][CH:21]=[CH:20][N:19]=1

Participants

3

Reactant 2

HCID 27340872-Bromo-4-methylpyridineHCID 87396686HCID 87396686, compound

Product 1

HCID 87396729HCID 87396729, compound

Procedure

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

Workup

  1. customThis compound is prepared by method C

Sources & evidence

ORD record
ord-1777ad17f3514b45801a0e5e3dbd8af3
Source dataset
uspto-grants-2011_10
Patent number
US08030339B2

Reaction notes

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