HCID 54041120, compound → HCID 53989773, compound
Reaction equation
C([O:8][C:9](=[O:50])[CH2:10][C@H:11]([NH:29][C:30](=[O:49])[CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][NH:36][C:37](=[O:48])[CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][NH:43][S:44]([CH3:47])(=[O:46])=[O:45])[C:12](=[O:28])[NH:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])C1C=CC=CC=1>CO>[CH3:47][S:44]([NH:43][CH2:42][CH2:41][CH2:40][CH2:39][CH2:38][C:37]([NH:36][CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][C:30]([NH:29][C@H:11]([C:12](=[O:28])[NH:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:10][C:9]([OH:50])=[O:8])=[O:49])=[O:48])(=[O:46])=[O:45]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
35 mg of the ester compound thus obtained was dissolved in 10 ml of methanol and after treating the mixture in the same manner as in Example 26, 110 mg of (S)-3-[6-(6-methanesulfonamidohexanamido)hexanamido]-3-tetradecylcarbamoylpropionic acid was obtained.
Workup
- additionafter treating the mixture in the same manner as in Example 26