Cyclopropylamine → 6-(1-cyclopropyl-4-phenyl-1H-imidazol-5-yl)-4-(methylthio)thieno[2,3-d]pyrimidine
Reaction equation
[CH2:1]([N:3]1[C:7]([C:8]2[S:18][C:11]3[N:12]=[CH:13][N:14]=[C:15]([S:16][CH3:17])[C:10]=3[CH:9]=2)=[C:6]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[N:5]=[CH:4]1)[CH3:2].[CH:25]1(N)CC1>>[CH:1]1([N:3]2[C:7]([C:8]3[S:18][C:11]4[N:12]=[CH:13][N:14]=[C:15]([S:16][CH3:17])[C:10]=4[CH:9]=3)=[C:6]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[N:5]=[CH:4]2)[CH2:25][CH2:2]1Participants
3
Procedure
The title compound was prepared by a similar process to that described for Intermediate 70 but using cyclopropylamine in place of ethylamine. Solid (25 mg, 14%) (contains 30% of 1-cyclopropyl-4,5-phenyl-1H-imidazole);
Sources & evidence
- ORD record
- ord-989f101a26004238aae7adec937d6677
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07427616B2
Reaction notes
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