Pyrrolidine → HCID 178479347, compound
Reaction equation
C(OC([NH:11][C@H:12]([C:20]([OH:22])=O)[CH2:13][CH2:14][CH2:15][NH:16][C:17](=[NH:19])[NH2:18])=O)C1C=CC=CC=1.[CH:23]1([S:28]([Cl:31])(=[O:30])=[O:29])[CH2:27][CH2:26][CH2:25][CH2:24]1.[NH:32]1[CH2:36][CH2:35][CH2:34][CH2:33]1>>[ClH:31].[NH:19]=[C:17]([NH:18][S:28]([CH:23]1[CH2:27][CH2:26][CH2:25][CH2:24]1)(=[O:30])=[O:29])[NH:16][CH2:15][CH2:14][CH2:13][C@@H:12]([C:20]([N:32]1[CH2:36][CH2:35][CH2:34][CH2:33]1)=[O:22])[NH2:11]Participants
4
Procedure
Starting from (S)-N2-(benzyloxycarbonyl)-arginine, cyclopentanesulphonyl chloride and pyrrolidine, the expected product is obtained according to the procedure described in Example 1.
Sources & evidence
- ORD record
- ord-57e0645d0f8545ae8927f3ed0ed64be4
- Source dataset
- uspto-grants-2004_04
- DOI