• English
  • 简体中文
Login Register
Current Location: Home > Feedback Help Print

【结 构 式】

【分子编号】36045

【品名】2-aminooctanoic acid

【CA登记号】

【 分 子 式 】C8H17NO2

【 分 子 量 】159.22852

【元素组成】C 60.35% H 10.76% N 8.8% O 20.1%

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:(I)

This compound can be obtained by two related ways: 1) The condensation of 2-aminooctanoic acid (I) with acetic anhydride in pyridine at 100 C gives 3-acetamidononan-2-one (III), which is hydrolyzed with refluxing aqueous concentrated HCl yielding 3-aminononan-2-one hydrochloride (IV). The reduction of (IV) with NaBH4 in methanol affords 3-amino-2-nonanol (V), which is condensed with 4,6-dichloro-5-aminopyrimidine (VI) by means of tributylamine in refluxing pentanol giving 5-amino-6-(2-hydroxy-3-nonylamino)-4-chloropyrimidine (VII). The cyclization of (VII) with ethyl orthoformate (A) by means of ethanesulfonic acid in refluxing CHCl3 affords 9-(2-hydroxy-3-nonyl)-6-chloropurine (VIII), which is finally hydrolyzed with refluxing aqueous 0.5 N NaOH. 2) The chloropurine (VIII) is treated with methanolic NH3 at 80-100 C in a pressure vessel to give 9-(2-hydroxy-3-nonyl)adenine (IX), which is then treated with NaNO2 in acetic acid aqueous HCl.

1 Giner-Sorolla, A. (Newport Pharmaceuticals International Inc.; Sloan-Kettering Institute); 9-(Hydroxy alkyl)purines. US 4221910 .
2 Simon, L.N.; Hadden, J.W. (Newport Pharmaceuticals International Inc.; Sloan-Kettering Institute); Method of imparting immunomodulating and antiviral activity. US 4221794 .
3 Serradell, M.N.; Blancafort, P.; Castaner, J.; Arrigoni-Martelli, E.; NPT-15,392. Drugs Fut 1983, 8, 5, 420.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(A) 21304 Triethyl orthoformate; 1-(Diethoxymethoxy)ethane; Diethoxymethyl ethyl ether 122-51-0 C7H16O3 详情 详情
(I) 36045 2-aminooctanoic acid C8H17NO2 详情 详情
(III) 36046 N-(1-acetylheptyl)acetamide C11H21NO2 详情 详情
(IV) 36047 3-amino-2-nonanone C9H19NO 详情 详情
(V) 36048 3-amino-2-nonanol C9H21NO 详情 详情
(VI) 22845 5-Amino-4,6-dichloropyrimidine; 4,6-dichloro-5-pyrimidinylamine; 4,6-dichloro-5-pyrimidinamine 5413-85-4 C4H3Cl2N3 详情 详情
(VII) 36049 3-[(5-amino-6-chloro-4-pyrimidinyl)amino]-2-nonanol C13H23ClN4O 详情 详情
(VIII) 36050 3-(6-chloro-9H-purin-9-yl)-2-nonanol C14H21ClN4O 详情 详情
(IX) 36051 3-(6-amino-9H-purin-9-yl)-2-nonanol C14H23N5O 详情 详情
Extended Information