반응식
[NH:1]1[C:5](=[O:6])[CH2:4][CH2:3][C@H:2]1[C:7]([OH:9])=O.C(N(CC)CC)C.C(Cl)(=O)C(C)(C)C.[O:24]([C@H:28]1[CH2:33][CH2:32][C@H:31]([NH2:34])[CH2:30][CH2:29]1)[N+:25]([O-:27])=[O:26]>O1CCCC1>[O:24]([C@H:28]1[CH2:29][CH2:30][C@H:31]([NH:34][C:7](=[O:9])[C@@H:2]2[CH2:3][CH2:4][C:5](=[O:6])[NH:1]2)[CH2:32][CH2:33]1)[N+:25]([O-:27])=[O:26]참가 물질
반응 조건
- 온도
- 5 °C
실험 절차
2.1 g (0.016 mol) (S)-pyroglutamic acid (2-pyrrolidinone-5-carboxylic acid) are dissolved in 50 ml abs. tetrahydrofuran and 2.5 ml (0.018 mol) triethylamine. With cooling to about 5° C., 2 ml (0.016 mol) pivaloyl chloride in 10 ml abs. tetrahydrofuran are added dropwise thereto. After 15 min stirring at 5° C., one adds dropwise thereto a solution of 3.9 g trans-4-nitroxycyclohexylamine in 40 ml abs. tetrahydrofuran and 2.8 ml (0.02 mol) triethylamine. Thereafter, one allows to stir for 2 d at room temperature, filters off with suction and removes the solvent in a vacuum. The residue is dissolved in ethyl acetate and shaken out with sodium hydrogen carbonate. After drying of the ethyl acetate phase with sodium sulphate, distilling off in a vacuum, trituration with ether and suction filtration, there remain 1.5 g of the title compound of the melting point 166° C., i.e. 35% of theory.
후처리
- additionone adds dropwise
- stirringto stir for 2 d at room temperature
- customremoves the solvent in a vacuum
- dissolutionThe residue is dissolved in ethyl acetate
- stirringshaken out with sodium hydrogen carbonate
- dry with materialAfter drying of the ethyl acetate phase with sodium sulphate
- distillationdistilling off in a vacuum, trituration with ether and suction filtration, there
출처 및 근거
- ORD 기록
- ord-0e8ccc6e6297482c98f7dbd1d0401946
- 출처 데이터셋
- uspto-grants-1995_05
- 특허 번호
- US05411989
연결된 노트
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