Trifluoroacetic acid → 2(R)-[(3,4-methylendioxybenzyl)-(2,6-dimethyl-4-methoxybenzenesulfonyl)amino]-3-[(2-pyrrol-1-yl)phenylcarbonylamino]-propionic acid

HRID 2298007ノート

反応式

HRID 2298007 の反応式
C([O:5][C:6](=[O:47])[C@H:7]([N:23]([CH2:37][C:38]1[CH:43]=[CH:42][C:41]2[O:44][CH2:45][O:46][C:40]=2[CH:39]=1)[S:24]([C:27]1[C:32]([CH3:33])=[CH:31][C:30]([O:34][CH3:35])=[CH:29][C:28]=1[CH3:36])(=[O:26])=[O:25])[CH2:8][NH:9][C:10]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[N:18]1[CH:22]=[CH:21][CH:20]=[CH:19]1)=[O:11])(C)(C)C.FC(F)(F)C(O)=O>FC(F)(F)C(O)=O.C(Cl)Cl>[CH2:45]1[O:44][C:41]2[CH:42]=[CH:43][C:38]([CH2:37][N:23]([S:24]([C:27]3[C:32]([CH3:33])=[CH:31][C:30]([O:34][CH3:35])=[CH:29][C:28]=3[CH3:36])(=[O:25])=[O:26])[C@H:7]([CH2:8][NH:9][C:10]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[N:18]3[CH:19]=[CH:20][CH:21]=[CH:22]3)=[O:11])[C:6]([OH:47])=[O:5])=[CH:39][C:40]=2[O:46]1

参加物

4

実験手順

A solution of tert-butyl-2(R)-[(3,4-methylendioxybenzyl)-(2,6-dimethyl-4-methoxybenzenesulfonyl)amino]-3-[(2-pyrrol-1-yl)phenylcarbonylamino]-propionate (915 mg, 1.3 mmol) in 20% trifluoracetic acid-methylene chloride (15 ml) was stirred for 1 hour. Extra trifluoroacetic acid (0.5 ml) was added and stirring continued for 1.5 hours. The material was then condensed on the rotary evaporator and the residue was taken up in toluene (40 ml) and again condensed. This procedure was repeated twice (2×40 ml toluene, to remove traces of trifluoracetic acid) to provide 2(R)-[(3,4-methylendioxybenzyl)-(2,6-dimethyl-4-methoxybenzenesulfonyl)amino]-3-[(2-pyrrol-1-yl)phenylcarbonylamino]-propionic acid as a golden tan solid (896 mg).

後処理

  1. customcondensed
  2. customon the rotary evaporator
  3. customagain condensed
  4. custom(2×40 ml toluene, to remove traces of trifluoracetic acid)

出典と根拠

ORDレコード
ord-aaf43d247faa49fe8870a29042204002
出典データセット
uspto-grants-2002_12
特許番号
US06492394B1

反応ノート

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