Pyrrolidine → HCID 21304791, compound
Reaction equation
C(OC([NH:11][CH2:12][CH2:13][CH2:14][C@@H:15]([C:24]([OH:26])=O)[NH:16]C(OC(C)(C)C)=O)=O)C1C=CC=CC=1.[CH:27]1([S:31]([Cl:34])(=[O:33])=[O:32])[CH2:30][CH2:29][CH2:28]1.[NH:35]1[CH2:39][CH2:38][CH2:37][CH2:36]1>>[ClH:34].[NH2:16][C@H:15]([C:24](=[O:26])[N:35]1[CH2:39][CH2:38][CH2:37][CH2:36]1)[CH2:14][CH2:13][CH2:12][NH:11][S:31]([CH:27]1[CH2:30][CH2:29][CH2:28]1)(=[O:33])=[O:32]Participants
4
Procedure
Starting from (S)-N5-(benzyloxycarbonyl)-N2-(tert-butyloxycarbonyl)-ornithine, cyclobutanesulphonyl chloride and pyrrolidine, the expected product is obtained according to the procedure described in Example 3.
Sources & evidence
- ORD record
- ord-d9063620f8bb4a0593bb8a4d54e23a1f
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06716843B2
Reaction notes
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