Hydrochloric Acid → 6-(Piperazin-1-yl)pyridine-3-carboxylic acid
반응식
C(OC([N:6]1[CH2:11][CH2:10][N:9]([C:12]2[CH:20]=[CH:19][C:15]([C:16]([OH:18])=[O:17])=[CH:14][N:13]=2)[CH2:8][CH2:7]1)=O)C.[OH-].[K+].Cl>O>[N:9]1([C:12]2[CH:20]=[CH:19][C:15]([C:16]([OH:18])=[O:17])=[CH:14][N:13]=2)[CH2:8][CH2:7][NH:6][CH2:11][CH2:10]1참가 물질
5
실험 절차
2.8 g of 6-(4-ethoxycarbonyl-1-piperazinyl)nicotinic acid obtained in Example 1 and 2 g of potassium hydroxide were dissolved in 20 ml of water. The solution was heated under reflux for 2 hours. After cooled, the reaction mixture was neutralized with concentrated hydrochloric acid and crystals precipitated were filtered, washed with water and dried to give 1.7 g of 6-(1-piperazinyl)nicotinic acid (yield 82%).
후처리
- temperatureThe solution was heated
- temperatureunder reflux for 2 hours
- temperatureAfter cooled
- customprecipitated
- filtrationwere filtered
- washwashed with water
- customdried
출처 및 근거
- ORD 기록
- ord-026e311ef5414df690d7f73bbcd7519f
- 출처 데이터셋
- uspto-grants-1991_06
- 특허 번호
- US05025012
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