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【结 构 式】

【分子编号】53618

【品名】2-methyl-1,3-benzoxazole-6-carbonyl azide

【CA登记号】n/a

【 分 子 式 】C9H6N4O2

【 分 子 量 】202.1724

【元素组成】C 53.47% H 2.99% N 27.71% O 15.83%

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 cyclization of 3aminopyridine (I) with diethyl ethoxymethylenemalonate (II) in refluxing Dowtherm gives 4-hydroxy-1,5-naphthyridine-3-carboxylic acid ethyl ester (III), which is hydrolyzed with NaOH in refluxing water to yield the corresponding hydroxyacid (IV). The decarboxylation of (IV) by heating at 320 C in mineral oil affords 4-hydroxy-1,5-naphthyridine (V), which is acylated with trifluoromethanesulfonic anhydride to provide the triflate (VI). The reaction of (VI) with propylamine in pyridine affords 4-amino-1,5-naphthyridine (VII), which is condensed with 2-methylbenzoxazole-6-ylcarbonyl azide (VIII) (obtained by reaction of the corresponding acid (IX) with DPPA) in refluxing toluene to provide the target urea.

1 Porter, R.A.; et al.; 1,3-Biarylureas as selective non-peptide antagonists of the orexin-1 receptor. Bioorg Med Chem Lett 2001, 11, 14, 1907.
2 Adams, J.T.; et al.; Synthesis of antimalarials. VI. Synthesis of certain 1,5- and 1,8-naphthyridine derivatives. J Am Chem Soc 1946, 68, 1317.
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) 33327 3-Pyridinylamine; 3-Aminopyridine; 3-Pyridinamine 462-08-8 C5H6N2 详情 详情
(II) 14088 Diethyl ethoxymethylenemalonate; Diethyl 2-(ethoxymethylene)malonate 87-13-8 C10H16O5 详情 详情
(III) 53616 ethyl 4-hydroxy[1,5]naphthyridine-3-carboxylate 13801-51-9 C11H10N2O3 详情 详情
(IV) 43932 4-hydroxy[1,5]naphthyridine-3-carboxylic acid C9H6N2O3 详情 详情
(V) 43933 [1,5]naphthyridin-4-ol C8H6N2O 详情 详情
(VI) 53617 [1,5]naphthyridin-4-yl trifluoromethanesulfonate n/a C9H5F3N2O3S 详情 详情
(VII) 43935 [1,5]naphthyridin-4-amine; [1,5]naphthyridin-4-ylamine C8H7N3 详情 详情
(VIII) 53618 2-methyl-1,3-benzoxazole-6-carbonyl azide n/a C9H6N4O2 详情 详情
(IX) 43936 2-methyl-1,3-benzoxazole-6-carboxylic acid C9H7NO3 详情 详情
Extended Information