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【结 构 式】

【分子编号】38882

【品名】4-[2-(dimethylamino)ethoxy]-5-isopropyl-2-methylphenyl 1-(3-methyl-3-sulfanylbutanoyl)-4-piperidinecarboxylate

【CA登记号】

【 分 子 式 】C25H40N2O4S

【 分 子 量 】464.66968

【元素组成】C 64.62% H 8.68% N 6.03% O 13.77% S 6.9%

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:(X)

Protection of 3-methyl-3-sulfanylbutanoic acid (I) by treatment with 2,4,6-trimethoxybenzyl alcohol (II) and trifluoroacetic acid produced the trimethoxybenzyl thioether (III). Subsequent coupling of (III) with ethyl isonipecotate (IV) using EDC and DMAP gave amide (V). The ethyl ester group of (V) was then hydrolyzed to carboxylic acid (VI) by means of ethanolic NaOH. This was then condensed with 4-[2-(dimethylamino)ethoxy]-2-methyl-5-isopropylphenol (VIII), prepared by basic hydrolysis of moxisylyte (VII), and the resulting ester (IX) was deprotected with trifluoroacetic acid to give thiol (X). Finally, S-nitrosation of (X) with tert-butyl nitrite, followed by treatment with succinic acid furnished the title compound.

1 Earl, R.A.; et al.; Nitrosylated alpha-adrenergic receptor antagonists as potential agents for the treatment of erectile dysfunction. 219th ACS Natl Meet (March 26 2000, San Francisco) 2000, Abst MEDI 239.
2 Gaston, R.D.; Saenz de Tejada, I.; Schroeder, J.D.; Shelekhin, T.E.; Garvey, D.S.; Wang, T. (NitroMed Inc.); Nitrosated and nitrosylated alpha-adrenergic receptor antagonists, compsns. and methods of use. WO 0012075 .
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) 32947 3-methyl-3-sulfanylbutyric acid C5H10O2S 详情 详情
(II) 38877 (2,4,6-trimethoxyphenyl)methanol C10H14O4 详情 详情
(III) 38878 3-methyl-3-[(2,4,6-trimethoxybenzyl)sulfanyl]butyric acid C15H22O5S 详情 详情
(IV) 17410 Ethyl isonipecotate; ethyl 4-piperidinecarboxylate 1126-09-6 C8H15NO2 详情 详情
(V) 38879 ethyl 1-[3-methyl-3-[(2,4,6-trimethoxybenzyl)sulfanyl]butanoyl]-4-piperidinecarboxylate C23H35NO6S 详情 详情
(VI) 38880 1-[3-methyl-3-[(2,4,6-trimethoxybenzyl)sulfanyl]butanoyl]-4-piperidinecarboxylic acid C21H31NO6S 详情 详情
(VII) 38875 4-[2-(dimethylamino)ethoxy]-5-isopropyl-2-methylphenyl acetate C16H25NO3 详情 详情
(VIII) 38876 4-[2-(dimethylamino)ethoxy]-5-isopropyl-2-methylphenol C14H23NO2 详情 详情
(IX) 38881 4-[2-(dimethylamino)ethoxy]-5-isopropyl-2-methylphenyl 1-[3-methyl-3-[(2,4,6-trimethoxybenzyl)sulfanyl]butanoyl]-4-piperidinecarboxylate C35H52N2O7S 详情 详情
(X) 38882 4-[2-(dimethylamino)ethoxy]-5-isopropyl-2-methylphenyl 1-(3-methyl-3-sulfanylbutanoyl)-4-piperidinecarboxylate C25H40N2O4S 详情 详情
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