Protoberberine의 고급지방산 유도체합성 및 활성연구(V)

• 영문명: Synthesis of Protoberberine Derivatives an Their Biological Activities
• 발행기관: 대한약학회
• 저자명: 김신규(Sin Kyu Kim) 권창호(Chang Ho Kwon) 육창수(Chang Soo Yook) 노영수(Young Soo Rho) 서성훈(Seong Hoon Seo) 정세영(Se Young Choung) 정성현(Sung Hyun Chung) 김동현(Dong Hyun Kim) 황순호(Soon Ho Hwang)
• 간행물 정보: 『약학회지』제36권 제1호 (1992년), 1~6쪽, 전체 6쪽
• 주제분류: 의약학 > 기타의약학
• 파일형태: PDF
• 발행일자: 1992.02.28

영문 초록

Irradiation of phenolbetaine in a stream of nitrogen produced 8,14-cycioberbine[1]. Compound[1] was treated with 10% HCl solution to give the 8,14-cycioberbine[2] in 67.7% yield. Subsequently addition of ethylchloroformate to the compound[2] gave rise to the 8-hydroxy-7-ethylcarboxy-9,10-dimethoxy-2,3-methylenelioxy-13-oxo-norochotensane[3] in 78% yield. Treatment of the compound[3] with bis-(2-chloroethyl)amine then lead to the 7-bis(2-chloroethyl)carbamyl-norochoteneare[4]. On the other hand the compound[5], which is the 8-methoxynorochotensane, was derived when compound[1] was treated with methanol in a few drops of BF. Treatment of the compound[6], and the compound[7], 7-bis(2-chloroethyl)-carbanyl-8-methoxy-norocheyensane, was then synthesized by reaction of the compound[6] with bis(2-choloroethyl) amine. In the other synthetic pathway when compound[5] was treated with POCl3 in dried benzene, 13-chloro-6-ene-norochetensane[8] with 42% yield was formed. Finally the 13-bis-(2-chloroethyl) amino-8-methoxy-norochotensane[9] was produced when we treated the compound[8] with bis-(2-chloroethyl) amine. In another pathway, reaction between phenolbetaine which is the precursor of the compound[1] and benzoylchloride in dried chloroform gave us the 5,6,7 trihydro-2,3-methylene-dioxy-9-chloromethyl-10,11-dimethoxyphenylisoquinoline-8-benzoate[10] in 73% yield. The results of biological activities for these compounds are also presented in Table I and II.