2-Bromo-3-methylthiophene → (4-Amino-2-ethylsulfanyl-pyrimidin-5-yl)-(3-methyl-thiophen-2-yl)-methanone
Reaction equation
CON(C)[C:4]([C:6]1[C:7]([NH2:15])=[N:8][C:9]([S:12][CH2:13][CH3:14])=[N:10][CH:11]=1)=[O:5].Br[C:18]1[S:19][CH:20]=[CH:21][C:22]=1[CH3:23]>>[NH2:15][C:7]1[C:6]([C:4]([C:18]2[S:19][CH:20]=[CH:21][C:22]=2[CH3:23])=[O:5])=[CH:11][N:10]=[C:9]([S:12][CH2:13][CH3:14])[N:8]=1Participants
3
Procedure
The compound was prepared from 4-amino-2-ethylsulfanyl-pyrimidine-5-carboxylic acid methoxy-methyl-amide, Example 1, and 2-bromo-3-methyl-thiophene (Aldrich) in an analogous manner as described in Example 169.
Sources & evidence
- ORD record
- ord-480eb2e1c1b34460a7bd82aeea679ca2
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07157455B2
Reaction notes
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