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【结 构 式】

【分子编号】17768

【品名】2-amino-N,N-ditetradecylacetamide

【CA登记号】

【 分 子 式 】C30H62N2O

【 分 子 量 】466.83516

【元素组成】C 77.19% H 13.39% N 6% O 3.43%

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)

Benzyloxycarbonylglycine (I) was coupled with N-hydroxysuccinimide in the presence of dicyclohexylcarbodiimide (DCC), and the resulting succinimidyl active ester (II) was condensed with dimiristylamine (III) to afford amide (IV). The benzyloxycarbonyl group was then removed by hydrogenolysis in the presence of palladium on carbon to yield amine (V). Coupling of this amine with Boc-protected L-arginine (VI) in the presence of diisopropylcarbodiimide (DIC) gave dipeptide (VII). Finally, partial deprotection of Boc groups with hydrochloric acid in dioxane provided the title compound.

1 Lewis, J.G.; et al.; A serum-resistant cytofectin for cellular delivery of antisense oligodeoxynucleotides and plasmid DNA. Proc Natl Acad Sci USA 1996, 93, 8, 3177.
2 Deprince, R.B.; Facchine, K.L.; Lewis, G.S.; Lewis, J.G.; Lin, K.-Y.; Matteucci, M.D.; Mook, R.A. Jr.; Wagner, R.W. (Gilead Sciences Inc.; Glaxo Wellcome plc); Cationic lipids for delivery of nucleic acids to cells. WO 9601841 .
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) 17764 N-Carbobenzyloxyglycine; 2-[[(benzyloxy)carbonyl]amino]acetic acid 1138-80-3 C10H11NO4 详情 详情
(II) 17765 benzyl 2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-2-oxoethylcarbamate; Z-glycine N-succinimidyl ester 2899-60-7 C14H14N2O6 详情 详情
(III) 17766 DITETRADECYLAMINE; N-tetradecyl-1-tetradecanamine; N,N-ditetradecylamine 17361-44-3 C28H59N 详情 详情
(IV) 17767 benzyl 2-(ditetradecylamino)-2-oxoethylcarbamate C38H68N2O3 详情 详情
(V) 17768 2-amino-N,N-ditetradecylacetamide C30H62N2O 详情 详情
(VI) 17769 (2S)-2-[(tert-butoxycarbonyl)amino]-5-[(tert-butoxycarbonyl)[imino(methylamino)methyl]amino]pentanoic acid C17H32N4O6 详情 详情
(VII) 17770 tert-butyl (4S)-4-[(tert-butoxycarbonyl)amino]-5-[[2-(ditetradecylamino)-2-oxoethyl]amino]-5-oxopentyl[[(tert-butoxycarbonyl)amino](imino)methyl]carbamate C51H98N6O8 详情 详情
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