HX-531
Chemical Name: 4-(2-Nitro-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-benzo[b]naptho[2,3-e][1,4]diazepin-12-yl)benzoic acid
项目整合开发状态: Preclinical
项目研究机构: University of Tokyo (Originator)
合成路线:Treatment of o-nitroaniline (I) with 6-bromo-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphtalene (II),K2CO3 and CuI in xylene yields diphenylamine derivative (III),which is then N-methylated by means of NaH and MeI in DMF to provide (IV).Reduction of the nitro group of (IV) by hydrogenation over Pd/C in ethanol or by treatment with Fe and HCl in H2O/EtOH affords the corresponding amine derivative (V),which is then condensed with terephthalic acid monomethyl ester chloride (VI) in benzene/pyridine to furnish compound (VII).Cyclization of (VII) by means of polyphosphoric acid (PPA) in CH2Cl2 gives diazepin derivative (VIII),which is finally converted in the target product by first nitration with KNO3 in H2SO4 followed by hydrolysis with NaOH in EtOH.
📌 参考资料/链接:
参考文献标题:Cpds.potentiating retinoid
文献作者:Shudo,K.(Nikken Chemicals Co.,Ltd.)
参考来源:JP 1998059951; US 5929069; US 6121256; WO 9711061
📄 详细内容
合成路线:Treatment of o-nitroaniline (I) with 6-bromo-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphtalene (II),K2CO3 and CuI in xylene yields diphenylamine derivative (III),which is then N-methylated by means of NaH and MeI in DMF to provide (IV).Reduction of the nitro group of (IV) by hydrogenation over Pd/C in ethanol or by treatment with Fe and HCl in H2O/EtOH affords the corresponding amine derivative (V),which is then condensed with terephthalic acid monomethyl ester chloride (VI) in benzene/pyridine to furnish compound (VII).Cyclization of (VII) by means of polyphosphoric acid (PPA) in CH2Cl2 gives diazepin derivative (VIII),which is finally converted in the target product by first nitration with KNO3 in H2SO4 followed by hydrolysis with NaOH in EtOH.
参考文献标题:Retinoid X receptor-antagonistic diazepinylbenzoic acids
文献作者:Ebisawa,M.; Umemiya,H.; Ohta,K.; Fukasawa,H.; Kawachi,E.; Christoffel,G.; Gronemeyer,H.; Tsuji,M.; Hashimoto,Y.; Shudo,K.; Kagechika,H.
参考来源:Chem Pharm Bull 1999,47(12),1778