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【结 构 式】

【分子编号】46807

【品名】5-[(8-hydroxy-1-naphthyl)oxy]-1,2,3,4-tetrahydro-1,8-naphthalenediol

【CA登记号】

【 分 子 式 】C20H18O4

【 分 子 量 】322.36052

【元素组成】C 74.52% H 5.63% O 19.85%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VIII)

Formation of ketal (III) is achieved by treatment of 5-hydroxy-8-methoxy-1-tetralone (I) with ethylene glycol (II) and pyridinium p-toluenesulfonate (PPTS) in benzene. Coupling of hydroxy derivative (III) with 8-iodo-1-methoxynaphthalene (IV) by means of Cu2O and K2CO3 in refluxing pyridine provides naphthyl ether (V), which is then hydrolyzed to ketone (VI) by means of TsOH in acetone/H2O. Demethylation of derivative (VI) is then performed by treatment with BBr3 in dichloromethane to yield hydroxy derivative (VII), which is reduced by means of LiAlH4 in Et2O to give triol (VIII). Oxidative cyclization of (VIII) using PhI(OAc)2 in trifluoroethanol affords naphthalene spiroketal (IX), which is converted into palmarumycin CP1 (X) by a two-step protocol consisting in a first oxidation with Dess-Martin periodane (and subsequent purification) followed by aromatization with MnO2 in dichloromethane. Finally, the target product is obtained by a Mitsunobu reaction of derivative (X) with alcohol (XI) using polystyrene-bound triphenylphosphine and DEAD in dichloromethane.

1 Wipf, P.; et al.; Synthesis and biological evaluation of deoxypreussomerin A and palmarumycin CP1 and related naphthoquinone spiroketals. Tetrahedron 2001, 57, 2, 283.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 46802 5-hydroxy-8-methoxy-3,4-dihydro-1(2H)-naphthalenone C11H12O3 详情 详情
(II) 11295 Polyethylene glycol;1,2-Ethanediol;Monoethylene glycol; Ethylene glycol 107-21-1 C2H6O2 详情 详情
(III) 46803   C13H16O4 详情 详情
(IV) 41878 8-iodo-1-naphthyl methyl ether; 1-iodo-8-methoxynaphthalene C11H9IO 详情 详情
(V) 46804   C24H24O5 详情 详情
(VI) 46805 8-methoxy-5-[(8-methoxy-1-naphthyl)oxy]-3,4-dihydro-1(2H)-naphthalenone C22H20O4 详情 详情
(VII) 46806 8-hydroxy-5-[(8-hydroxy-1-naphthyl)oxy]-3,4-dihydro-1(2H)-naphthalenone C20H16O4 详情 详情
(VIII) 46807 5-[(8-hydroxy-1-naphthyl)oxy]-1,2,3,4-tetrahydro-1,8-naphthalenediol C20H18O4 详情 详情
(IX) 46808   C20H16O4 详情 详情
(X) 46809   C20H12O4 详情 详情
(XI) 13848 2-Furylmethanol; Furfuryl Alcohol 98-00-0 C5H6O2 详情 详情
Extended Information