Ammonia → trans-1-(p-nitrobenzyloxycarbonyl)-4-hydroxy-L-prolineamide
反応式
[N+:1]([C:4]1[CH:22]=[CH:21][C:7]([CH2:8][O:9][C:10]([N:12]2[CH2:19][C@H:18]([OH:20])[CH2:17][C@H:13]2[C:14](O)=[O:15])=[O:11])=[CH:6][CH:5]=1)([O-:3])=[O:2].C([N:25](CC)CC)C.ClC(OCC)=O.N>O1CCCC1>[N+:1]([C:4]1[CH:22]=[CH:21][C:7]([CH2:8][O:9][C:10]([N:12]2[CH2:19][C@H:18]([OH:20])[CH2:17][C@H:13]2[C:14]([NH2:25])=[O:15])=[O:11])=[CH:6][CH:5]=1)([O-:3])=[O:2]参加物
実験手順
3.10 g of trans-1-(p-nitrobenzyloxycarbonyl)-4-hydroxy-L-proline and 1.10 g of triethylamine were dissolved in 40 ml of dried tetrahydrofuran, and a solution of 1.20 g of ethyl chloroformate in 10 ml of dried tetrahydrofuran was added dropwise thereto at -25° C. to -35° C. After stirring at the same temperature for 50 minutes, 10 ml of concentrated aqueous ammonia was added dropwise to the mixture at -25° to -40° C. The temperature was then gradually elevated to room temperature, and the reaction mixture was stirred for 1 hour, followed by concentration under reduced pressure. To the residue were added 20 ml of water and 50 ml of diethyl ether. After ice-cooling, the thus formed white crystals were separated by filtration, washed successively with cool water and cool diethyl ether, and dried under reduced pressure to yield trans-1-(p-nitrobenzyloxycarbonyl)-4-hydroxy-L-prolineamide.
後処理
- customat -25° C. to -35° C
- customwas then gradually elevated to room temperature
- stirringthe reaction mixture was stirred for 1 hour
- concentrationfollowed by concentration under reduced pressure
- additionTo the residue were added 20 ml of water and 50 ml of diethyl ether
- temperatureAfter ice-cooling
- customthe thus formed white crystals were separated by filtration
- washwashed successively with cool water
- temperaturecool diethyl ether
- customdried under reduced pressure
出典と根拠
- ORDレコード
- ord-ec0dc1fa9c2147748c5d6921c8bf4c14
- 出典データセット
- uspto-grants-1990_07
- 特許番号
- US04943569
反応ノート
読み込み中…