反応式
[CH2:1]([O:8][C:9](=[O:23])[CH2:10][C@@H:11]([C:20](O)=[O:21])[NH:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN1CCOCC1.ClC(OCC(C)C)=O>C(COC)OC>[C:16]([O:15][C:13]([NH:12][C@H:11]([CH2:20][OH:21])[CH2:10][C:9]([O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[O:23])=[O:14])([CH3:18])([CH3:19])[CH3:17]参加物
反応条件
- 温度
- -5 °C
実験手順
N-(tert-Butoxycarbonyl)-L-aspartic acid 4-benzyl ester (30 g) was dissolved in dimethoxyethane (90 mL) and the solution was cooled to −5° C. N-Methylmorpholine (10.32 mL) was added followed by isobutyl chloroformate (12.7 mL) in such a way to keep the temperature below −10° C. The mixture was aged for 0.5 hour. The solids were quickly filtered and washed with dimethoxyethane (90 mL). To the filtrate cooled to −50° C. was carefully added sodium borohydride (4.4 g) as a solution in water (45 mL) in such a way to keep the temperature between −30° C. and −15° C. After all the hydride had been added, water (500 mL) was added in such a way to maintain the temperature below −15° C. The suspension was filtered, the solid washed with water (400 mL) and dried to yield benzyl (3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutanoate.
後処理
- customthe temperature below −10° C
- filtrationThe solids were quickly filtered
- washwashed with dimethoxyethane (90 mL)
- temperatureTo the filtrate cooled to −50° C.
- customthe temperature between −30° C. and −15° C
- additionAfter all the hydride had been added
- additionwater (500 mL) was added in such a way
- temperatureto maintain the temperature below −15° C
- filtrationThe suspension was filtered
- washthe solid washed with water (400 mL)
- customdried
出典と根拠
- ORDレコード
- ord-4836e393f561456bb61829e49fc1c52c
- 出典データセット
- uspto-grants-2007_12
- 特許番号
- US07312353B2
関連ノート
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