(2S,4R)-4-(2-chlorophenylsulfonyl)-N-(1-cyanocyclopropyl)pyrrolidine-2-carboxamide → HCID 71711169, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([C@H:11]1[CH2:15][NH:14][C@H:13]([C:16]([NH:18][C:19]2([C:22]#[N:23])[CH2:21][CH2:20]2)=[O:17])[CH2:12]1)(=[O:10])=[O:9].Cl.[N:25]1([C:30]2([C:33](O)=[O:34])[CH2:32][CH2:31]2)[CH2:29][CH2:28][CH2:27][CH2:26]1>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([C@H:11]1[CH2:15][N:14]([C:33]([C:30]2([N:25]3[CH2:29][CH2:28][CH2:27][CH2:26]3)[CH2:32][CH2:31]2)=[O:34])[C@H:13]([C:16]([NH:18][C:19]2([C:22]#[N:23])[CH2:21][CH2:20]2)=[O:17])[CH2:12]1)(=[O:10])=[O:9]Participants
3
Procedure
The reaction of (2S,4R)-4-(2-chlorophenylsulfonyl)-N-(1-cyanocyclopropyl)pyrrolidine-2-carboxamide 7H with 1-(pyrrolidin-1-yl)cyclopropanecarboxylic acid hydrochloride 16D carried out according to the general procedure L yielded (2S,4R)-4-(2-chlorophenylsulfonyl)-N-(1-cyanocyclopropyl)-1-(1-(pyrrolidin-1-yl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide as a yellow solid (41%). MS ISP (m/e): 491.2 (100) [(M+H)]+.
Sources & evidence
- ORD record
- ord-028767ffd3f740fca73aba97a4715275
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08802665B2
Reaction notes
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