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【结 构 式】

【分子编号】64763

【品名】cyclopropylmethanol

【CA登记号】

【 分 子 式 】C4H8O

【 分 子 量 】72.10692

【元素组成】C 66.63% H 11.18% O 22.19%

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:(VIII)

The condensation of 2-chloropyridine (I) with ethyl trifluoroacetate (II) by means of LDA in THF gives 2-chloro-3-(trifluoroacetyl)pyridine (III), which is condensed with 4-fluoroaniline (IV) by means of refluxing aqueous acetic acid to yield the diarylamine (V). The cyclization of (V) by means of concentrated H2SO4 affords 7-fluoro-5-hydroxy-5-(trifluoromethyl)-5,10-dihydro-benzo[b]-1,8-naphthyridine (VI), which is dehydrated in THF to give 7-fluoro-5-(trifluoromethyl)benzo[b]-1,8-naphthyridine (VII). The condensation of (VII) with cyclopropylmethanol (VIII) by means of anhydrous HCl in dichloromethane yields the 5-(cyclopropylmethoxy)-7-fluoro-5-(trifluoromethyl)-5,10-dihydro-benzo[b]-1,8-naphthyridine (IX), which is oxidated by means of MCPBA in dichloromethane to afford the N-oxide (X) (1, 2). Finally, this racemic compound is submitted to chiral HPLC to obtain the target enantiomer (1).

1 Novel 5,10-dihydrobenzo[B][1,8]napthyridine N-oxides as non-nucleoside reverse transcriptase inhibitors of HIV-1 with high potency against clinically relevant mutants variants. 226th ACS Natl Meet (Sept 7 2003, New York) 2003, Abst MEDI 129.
2 Patel, M.; Rodgers, J.D.; Wang, H.; Johnson, B.L. (Bristol-Myers Squibb Co.); Tricyclic cpds. useful as HIV reverse transcriptase inhibitors. JP 2003512375; US 6593337; WO 0129037 .
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) 17503 2-chloropyridine 109-09-1 C5H4ClN 详情 详情
(II) 14588 Ethyl 2,2,2-trifluoroacetate; Trifluoroethyl acetate 383-63-1 C4H5F3O2 详情 详情
(III) 64759 1-(2-chloro-3-pyridinyl)-2,2,2-trifluoro-1-ethanone C7H3ClF3NO 详情 详情
(IV) 37690 4-fluorophenylamine; 4-fluoroaniline 371-40-4 C6H6FN 详情 详情
(V) 64760 2,2,2-trifluoro-1-[2-(4-fluoroanilino)-3-pyridinyl]-1-ethanone C13H8F4N2O 详情 详情
(VI) 64761 7-fluoro-5-(trifluoromethyl)-5,10-dihydrobenzo[b][1,8]naphthyridin-5-ol C13H8F4N2O 详情 详情
(VII) 64762 7-fluoro-5-(trifluoromethyl)benzo[b][1,8]naphthyridine C13H6F4N2 详情 详情
(VIII) 64763 cyclopropylmethanol C4H8O 详情 详情
(IX) 64764 5-(cyclopropylmethoxy)-7-fluoro-5-(trifluoromethyl)-5,10-dihydrobenzo[b][1,8]naphthyridine; cyclopropylmethyl 7-fluoro-5-(trifluoromethyl)-5,10-dihydrobenzo[b][1,8]naphthyridin-5-yl ether C17H14F4N2O 详情 详情
(X) 64765 5-(cyclopropylmethoxy)-7-fluoro-5-(trifluoromethyl)-5,10-dihydrobenzo[b][1,8]naphthyridin-1-ium-1-olate C17H14F4N2O2 详情 详情
Extended Information