2-(3-chlorophenyl)benzoic Acid → 6-methyl-imidazo[2,1-b]thiazole-5-carboxylic acid [(1S,3S,5S)-2-(3'-chloro-biphenyl-2-carbonyl)-2-aza-bicyclo[3.1.0]hex-3-ylmethyl]-amide
Reaction equation
[C@H:1]12[CH2:6][C@H:5]1[CH2:4][C@@H:3]([CH2:7][NH:8][C:9]([C:11]1[N:18]3[C:14]([S:15][CH:16]=[CH:17]3)=[N:13][C:12]=1[CH3:19])=[O:10])[NH:2]2.[Cl:20][C:21]1[CH:22]=[C:23]([C:27]2[C:28]([C:33](O)=[O:34])=[CH:29][CH:30]=[CH:31][CH:32]=2)[CH:24]=[CH:25][CH:26]=1>>[Cl:20][C:21]1[CH:22]=[C:23]([C:27]2[C:28]([C:33]([N:2]3[C@H:3]([CH2:7][NH:8][C:9]([C:11]4[N:18]5[C:14]([S:15][CH:16]=[CH:17]5)=[N:13][C:12]=4[CH3:19])=[O:10])[CH2:4][C@H:5]4[C@@H:1]3[CH2:6]4)=[O:34])=[CH:29][CH:30]=[CH:31][CH:32]=2)[CH:24]=[CH:25][CH:26]=1Participants
3
Reactant 2
Product 1
Procedure
prepared by reaction of 6-methyl-imidazo[2,1-b]thiazole-5-carboxylic acid [(1S,3S,5S)-2-aza-bicyclo[3.1.0]hex-3-ylmethyl]-amide with 3′-chloro-biphenyl-2-carboxylic acid. LC-MS (basic): tR=1.38 min; [M+H]+=490.9.
Sources & evidence
- ORD record
- ord-2f77de44491244339de8e94dd445b1f1
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288435B2
Reaction notes
Loading…