2-Azetidinecarboxylic acid, (S)- → (S)-1,10a-dihydro-5-methyl-2H-azeto[2,1-c][1,4]benzodiazepine-4,10(9H)-dione
반응식
[CH2:1]1[C@@H:4]([C:5]([OH:7])=O)[NH:3][CH2:2]1.[CH3:8][C:9]1[CH:10]=[CH:11][CH:12]=[C:13]2[NH:19]C(=O)O[C:15](=[O:16])[C:14]=12>CS(C)=O>[CH3:8][C:9]1[C:14]2[C:15](=[O:16])[N:3]3[CH2:2][CH2:1][C@H:4]3[C:5](=[O:7])[NH:19][C:13]=2[CH:12]=[CH:11][CH:10]=1참가 물질
4
실험 절차
13.0 g (128.4 mmol) of L-azetidine-2-carboxylic acid and 22.7 g (128.4 mmol) of 6-methyl-isatoic acid anhydride in 150 ml of dimethyl sulphoxide are heated to 95° for 3 hours, evaporated to dryness in a high vacuum and the residue obtained is heated to 140° for 2.25 hours. By crystallization from ethyl acetate there is obtained (S)-1,10a-dihydro-5-methyl-2H-azeto[2,1-c][1,4]benzodiazepine-4,10(9H)-dione of melting point 159°-160°.
후처리
- customevaporated to dryness in a high vacuum
- customthe residue obtained
- temperatureis heated to 140° for 2.25 hours
- customBy crystallization from ethyl acetate
출처 및 근거
- ORD 기록
- ord-977c01afaf7e419d8ad27442cd1f15fb
- 출처 데이터셋
- uspto-grants-1984_12
- 특허 번호
- US04489003
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