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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 231313생성일: 2026년 10월 23일

Sodium Bicarbonate → 2-[4-(1,2,3,4-Tetrahydro-8-hydroxy-2-naphthalenyl)-1-piperazinyl]pyrimidine

https://huagongshe.com/ko/reaction/231313

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물BoronHCID 5462311—
반응물2-(4-(1,2,3,4-Tetrahydro-8-methoxy-2-naphthalenyl)-1-piperazinyl]-pyrimidine hydrochlorideHCID 14479999—
용매DichloromethaneHCID 6344—
생성물2-[4-(1,2,3,4-Tetrahydro-8-hydroxy-2-naphthalenyl)-1-piperazinyl]pyrimidineHCID 1448000270.9%

반응 조건

온도-78 °C

반응 단계

2-(4-(1,2,3,4-Tetrahydro-8-methoxy-2-naphthalenyl)-1-piperazinyl]-pyrimidine hydrochloride (1.62 g, 5.0 mmole) was dissolved in 185 ml of methylene chloride and cooled to -78° C. in a dry ice/acetone bath. A mixture of 15 ml of 1 M boron triboromide and 15 ml of methylene chloride was added. The reaction mixture was allowed to come to room temperature and it was then stirred for three days. The reaction was then poured into a saturated NaHCO3 solution and the product extracted with 600 ml of chloroform. This solution was dried over MgSO4, filtered, and concentrated in vacuum. The residue was column chromatographed on 100 g of silica gel with 5% methanol/chloroform and the crude title compound thus obtained was crystallized from isopropanol with addition of 4 N isopropanolic HCl and recrystallized from acetone to give 1.1 g of the title compound as the hydrochloride, monohydrate, m.p.>300° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04845221
출처 데이터셋uspto-grants-1989_07
ORD IDord-9d94aa52a6f94522be50fbb6f5df93e1
출처 메모uspto-grants-1989_07