Methyl((1,3-thiazol-2-yl)methyl)amine → N-Methyl-N-thiazol-2-ylmethyl-6-[5-(2-trifluoromethylbenzoyl)-3,4,5,6-tetrahydro-1H-pyrrolo[3,4-c]pyrrol-2-yl]nicotinamide
Reaction equation
[F:1][C:2]([F:29])([F:28])[C:3]1[CH:27]=[CH:26][CH:25]=[CH:24][C:4]=1[C:5]([N:7]1[CH2:11][C:10]2[CH2:12][N:13]([C:15]3[CH:23]=[CH:22][C:18]([C:19]([OH:21])=O)=[CH:17][N:16]=3)[CH2:14][C:9]=2[CH2:8]1)=[O:6].[CH3:30][NH:31][CH2:32][C:33]1[S:34][CH:35]=[CH:36][N:37]=1>>[CH3:30][N:31]([CH2:32][C:33]1[S:34][CH:35]=[CH:36][N:37]=1)[C:19](=[O:21])[C:18]1[CH:22]=[CH:23][C:15]([N:13]2[CH2:14][C:9]3[CH2:8][N:7]([C:5](=[O:6])[C:4]4[CH:24]=[CH:25][CH:26]=[CH:27][C:3]=4[C:2]([F:1])([F:29])[F:28])[CH2:11][C:10]=3[CH2:12]2)=[N:16][CH:17]=1Participants
3
Reactant 2
Product 1
Procedure
6-[5-(2-Trifluoromethylbenzoyl)-3,4,5,6-tetrahydro-1H-pyrrolo[3,4-c]pyrrol-2-yl]nicotinic acid (54 mg, 0.134 mmol) was reacted with methylthiazol-2-ylmethylamine analogously to example 3d. Yield: 52%, M+H+: 514.30.
Sources & evidence
- ORD record
- ord-c646f6a55c434c1d85343d906792bcc5
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08003677B2
Reaction notes
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