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【结 构 式】

【分子编号】46778

【品名】(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl [(2S)-5-methoxy-1,2,3,4-tetrahydro-2-naphthalenyl]methyl carbonate

【CA登记号】

【 分 子 式 】C23H34O4

【 分 子 量 】374.52056

【元素组成】C 73.76% H 9.15% O 17.09%

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:(V)

Dehydroxylation of compound (I) by hydrogenation over Pd/C in MeOH provides tetralinecarboxylic acid methyl ester (II), which is then reduced by means of LiAlH4 in THF to afford tetralinemethanol as a mixture of enantiomers (III). Separation of isomers in (III) is then achieved by first acylation of the alcohol with (-)-menthyl chloroformate (IV) in pyridine, followed by the separation of the two resulting diastereomers by recrystallization to give (-)-menthyl carbonate (V) and its subsequent hydrolysis with NaOH in THF/H2O to furnish compound (VI).

1 Tsubaki, K.; Hattori, K.; Tabuchi, S.; Okitsu, O.; Sakane, K.; Tanaka, H.; Taniguchi, K.; A novel pyridazinone derivative as a nonprostanoid PGI2 agonist. Bioorg Med Chem Lett 2000, 10, 24, 2787.
2 Taniguchi, K.; Nagano, M.; Hattori, K.; Tsubaki, K.; Okitsu, O.; Tabuchi, S. (Fujisawa Pharmaceutical Co., Ltd.); Naphthalene derivs. as prostaglandin I2 agonists. EP 0749424; JP 1997509958; US 5763489; WO 9524393 .
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) 46774 methyl (1R,2S)-1-hydroxy-5-methoxy-1,2,3,4-tetrahydro-2-naphthalenecarboxylate C13H16O4 详情 详情
(II) 46775 methyl (2S)-5-methoxy-1,2,3,4-tetrahydro-2-naphthalenecarboxylate C13H16O3 详情 详情
(III) 46776 (5-methoxy-1,2,3,4-tetrahydro-2-naphthalenyl)methanol C12H16O2 详情 详情
(IV) 46777 (1S,2R,4R)-2-[(chlorocarbonyl)oxy]-1-isopropyl-4-methylcyclohexane 14602-86-9 C11H19ClO2 详情 详情
(V) 46778 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl [(2S)-5-methoxy-1,2,3,4-tetrahydro-2-naphthalenyl]methyl carbonate C23H34O4 详情 详情
(VI) 46779 [(2S)-5-methoxy-1,2,3,4-tetrahydro-2-naphthalenyl]methanol C12H16O2 详情 详情
(VII) 46780 1,1-diphenylacetone 781-35-1 C15H14O 详情 详情
(VIII) 15618 2-Oxoacetic acid; Glyoxylic Acid 298-12-4 C2H2O3 详情 详情
(IX) 46781 2-hydroxy-4-oxo-5,5-diphenylpentanoic acid C17H16O4 详情 详情
(X) 46782 6-benzhydryl-1,6-dihydro-3(2H)-pyridazinone C17H16N2O 详情 详情
(XI) 46783 6-benzhydryl-2-[[(2S)-5-methoxy-1,2,3,4-tetrahydro-2-naphthalenyl]methyl]-1,6-dihydro-3(2H)-pyridazinone C29H30N2O2 详情 详情
(XII) 46784 6-benzhydryl-2-[[(2S)-5-hydroxy-1,2,3,4-tetrahydro-2-naphthalenyl]methyl]-1,6-dihydro-3(2H)-pyridazinone C28H28N2O2 详情 详情
(XIII) 16640 Ethyl 2-bromoacetate; Ethyl bromoacetate 105-36-2 C4H7BrO2 详情 详情
(XIV) 46785 ethyl 2-[((6S)-6-[[3-benzhydryl-6-oxo-3,6-dihydro-1(2H)-pyridazinyl]methyl]-5,6,7,8-tetrahydro-1-naphthalenyl)oxy]acetate C32H34N2O4 详情 详情
Extended Information