Potassium Hydroxide → 1-Cyclopentyl-6-methylergoline-8-carboxylic acid
반응식
[CH3:1][N:2]1[CH:7]2[CH2:8][C:9]3[C:17]4[C:12](=[CH:13][CH:14]=[CH:15][C:16]=4[CH:6]2[CH2:5][CH:4]([C:18]([OH:20])=[O:19])[CH2:3]1)[NH:11][CH:10]=3.[OH-].[K+].C1(C)C=CC(S(O[CH:33]2[CH2:37][CH2:36][CH2:35][CH2:34]2)(=O)=O)=CC=1>CS(C)=O>[CH:33]1([N:11]2[C:12]3[C:17]4[C:9]([CH2:8][C@@H:7]5[C@@H:6]([C:16]=4[CH:15]=[CH:14][CH:13]=3)[CH2:5][CH:4]([C:18]([OH:20])=[O:19])[CH2:3][N:2]5[CH3:1])=[CH:10]2)[CH2:37][CH2:36][CH2:35][CH2:34]1참가 물질
실험 절차
To a 500 ml, three-neck round bottom flask was added 10.0 g (33.9 mmol) of 92% pure 9,10-dihydrolysergic acid, 11.72 g (180.0 mmol) of 86% pure powdered potassium hydroxide and 150 ml of DMSO. The mixture was stirred for 15 minutes and 10.22 g (42.6 mmol) of p-toluenesulfonic acid, cyclopentyl ester was added. The mixture was stirred at room temperature for about 20 hours and an additional 3.11 g (13.0 mmol) of p-toluenesulfonic acid, cyclopentyl ester was added. The mixture was stirred for an additional two hours and was poured into 750 ml of ice water. The mixture was washed twice with 200 ml portions of ethyl acetate and the pH of the aqueous phase was lowered to about 5 with glacial acetic acid. The mixture was cooled and the precipitated solid was collected by vacuum filtration. The solid was washed with water and dried under vacuum to provide 10.05 g of the title compound having a purity of 96.3 %. Yield 85.2%. Exact mass: theory 339.20725; found 339.20633.
후처리
- stirringThe mixture was stirred at room temperature for about 20 hours
- stirringThe mixture was stirred for an additional two hours
- washThe mixture was washed twice with 200 ml portions of ethyl acetate
- temperatureThe mixture was cooled
- filtrationthe precipitated solid was collected by vacuum filtration
- washThe solid was washed with water
- customdried under vacuum
출처 및 근거
- ORD 기록
- ord-f575fdb960b541dbb85960bef338f33e
- 출처 데이터셋
- uspto-grants-1988_03
- 특허 번호
- US04734501
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