HCID 54041120、化合物 → HCID 53989773、化合物
反応式
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]参加物
3
実験手順
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.
後処理
- additionafter treating the mixture in the same manner as in Example 26
出典と根拠
- ORDレコード
- ord-a2cd63468c1f44e5adb8b71074dfd812