反応式
[NH2:1][C@@H:2]1[C:8](=[O:9])[N:7]([CH2:10][C:11](OCC)=[O:12])[C:6]2[CH:16]=[CH:17][CH:18]=[CH:19][C:5]=2[S:4][C@H:3]1[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.[CH2:26]1[CH:31]([C:32]([OH:34])=O)[CH2:30][C:28](=[O:29])[CH2:27]1.O[N:36]1C2C=CC=CC=2N=N1.C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C=O>[C@@H:31]1([C:32]([NH:1][C@@H:2]2[C:8](=[O:9])[N:7]([CH2:10][C:11]([NH2:36])=[O:12])[C:6]3[CH:16]=[CH:17][CH:18]=[CH:19][C:5]=3[S:4][C@H:3]2[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)=[O:34])[CH2:26][CH2:27][C:28](=[O:29])[CH2:30]1参加物
実験手順
To a solution of 10 ml of dry dimethylformamide of 511 mg of ethyl 3(R)-amino-4-oxo-2(S)-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate, 200 mg of 3-cyclopentanone-1(R)-carboxylic acid which is prepared according to the known procedure and 322 mg of 1-hydroxybenzotriazole is added 322 mg of dicyclohexylcarbodiimide. After allowing to stand overnight, the precipitated dicyclohexylurea is filtered off. The dimethylformamide was distilled off under reduced pressure, and to the residue is added chloroform. After washing with an aqueous solution of sodium chloride and drying over magnesium sulfate, the solvent is distilled off. The residue is subjected to column chromatography on silica gel and crystallized from benzene to give 540 ml of 3(R)-[3-cyclopentanone-1(R)-carboxamido]-4-oxo-2(S)-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetamide, m.p.=135°- 150° C.
後処理
- filtrationthe precipitated dicyclohexylurea is filtered off
- distillationThe dimethylformamide was distilled off under reduced pressure
- additionto the residue is added chloroform
- washAfter washing with an aqueous solution of sodium chloride
- dry with materialdrying over magnesium sulfate
- distillationthe solvent is distilled off
- customcrystallized from benzene
出典と根拠
- ORDレコード
- ord-dd6ac23e2d124db0b2453634674fe2e4
- 出典データセット
- uspto-grants-1991_10
- 特許番号
- US05055464
関連ノート
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