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【结 构 式】

【分子编号】43262

【品名】10-undecenylamine; 10-undecen-1-amine

【CA登记号】

【 分 子 式 】C11H23N

【 分 子 量 】169.31036

【元素组成】C 78.03% H 13.69% N 8.27%

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:(IV)

Conversion of 10-undecen-1-ol (I) into the primary amine (IV) was effected by Mitsunobu coupling of (I) with phthalimide (II), followed by hydrazinolysis of the resulting N-(10-undecenyl)phthalimide (III). Amine (IV) was then acylated with O-acetylsalicyloyl chloride (V) to give salicylamide (VI). Oxidative cleavage of the terminal olefin to the carboxylic acid (VII) was achieved using potassium permanganate under phase-transfer conditions. The O-acetyl group was finally removed by treatment with NaOH.

1 Leone-Bay, A.; Paton, D.R.; Freeman, J.; et al.; Synthesis and evaluation of compounds that facilitate the gastrointestinal absorption of heparin. J Med Chem 1998, 41, 7, 1163.
2 Leone-Bay, A.; Ho, K.-K.; Sarubbi, D.J.; Milstein, S.J.; Press, J.B. (Emisphere Technologies, Inc.); Cpds. and compsns. for delivering active agents. US 5650386; WO 9630036 .
3 Leone-Bay, A. (Emisphere Technologies, Inc.); Cpds. and compsns. for delivering active agents. WO 9736480 .
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) 43260 10-undecen-1-ol 112-43-6 C11H22O 详情 详情
(II) 12376 Phthalimide; 1H-Isoindole-1,3(2H)-dione; Isoindole-1,3-dione;Phthalic dicarboximide;Phenylimide;Isoindole-1,3-dione 85-41-6 C8H5NO2 详情 详情
(III) 43261 2-(10-undecenyl)-1H-isoindole-1,3(2H)-dione C19H25NO2 详情 详情
(IV) 43262 10-undecenylamine; 10-undecen-1-amine C11H23N 详情 详情
(V) 16900 2-(chlorocarbonyl)phenyl acetate; Acetylsalicyloyl chloride 5538-51-2 C9H7ClO3 详情 详情
(VI) 43263 2-[(10-undecenylamino)carbonyl]phenyl acetate C20H29NO3 详情 详情
(VII) 43264 10-[[2-(acetoxy)benzoyl]amino]decanoic acid C19H27NO5 详情 详情
Extended Information