Thiazole, 2-(phenylthio)- → 5-Bromo-2-chloro-4-[2-(phenylthio)thiazol-5-yl]pyrimidine
Reaction equation
[C:1]1([S:7][C:8]2[S:9][CH:10]=[CH:11][N:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:13][C:14]1[CH:15]=[N:16][C:17]([Cl:20])=[N:18][CH:19]=1>>[Br:13][C:14]1[C:15]([C:10]2[S:9][C:8]([S:7][C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)=[N:12][CH:11]=2)=[N:16][C:17]([Cl:20])=[N:18][CH:19]=1Participants
3
Procedure
The title compound was prepared from 2-Phenylthiothiazole and 5-bromo-2-chloro-pyrimidine in a manner analogous to Example 249, Step 1. MS (M+H)+ 386.
Sources & evidence
- ORD record
- ord-120a789a56d64386b59fb4ef88c21080
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07786132B2
Reaction notes
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