tert-butyl N-(3-{[(2R,3S,4S,4aS,8aS)-4-[(3,5-dihydroxyphenyl)carbonyl]-3,4a,8,8-tetramethyldecahydronaphthalen-2-yl]amino}propyl)carbamate 、
盐酸 在
甲醇 、
乙醚 作用下,
以
异丙醇 为溶剂,
反应 18.5h,
以to afford 5-{[(1S,2S,3R,4aS,8aS)-3-[(3-aminopropyl)amino]-2,5,5,8a-tetramethyl-decahydronaphthalen-1-yl]carbonyl}benzene-1,3-diol dihydrochloride as a colourless solid (Compound No的产率得到5-{[(1S,2S,3R,4aS,8aS)-3-[(3-aminopropyl)amino]-2,5,5,8a-tetramethyl-decahydronaphthalen-1-yl]carbonyl}benzene-1,3-diol dihydrochloride