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【结 构 式】

【分子编号】25086

【品名】1-(7-amino-2-methyl-1-benzofuran-3-yl)-1-ethanone

【CA登记号】

【 分 子 式 】C11H11NO2

【 分 子 量 】189.21388

【元素组成】C 69.83% H 5.86% N 7.4% O 16.91%

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)

The condensation of 2-fluoronitrobenzene (I) with acetone oxime (II) by means of NaH in DMF gives acetone O-(2-nitrophenyl)oxime (III), which is cyclized to 2-methyl-7-nitrobenzofuran (IV) by means of H2SO4. The Friedel Crafts acylation of (IV) with acetyl chloride and AlCl3 in dichloromethane affords 3-acetyl-2-methyl-7-nitrobenzofuran (V), which is reduced to the corresponding amino derivative (VI) with Fe and HCl in ethanol. The condensation of (VI) with 2,6-dichlorobenzoyl chloride (VII) by means of triethylamine in dichloroethane yields N-(3-acetyl-2-methylbenzofuran-7-yl)-2,6-dichlorobenzamide (VIII), which is finally submitted to a Grignard reaction with methylmagnesium bromide in THF.

1 Yamazaki, H.; et al.; Synthesis and pharmacological activities of novel benzofuran derivatives as vacuolar type H+-ATPase inhibitors. Symp Med Chem 1998, Abst 2-P-32.
2 Kawai, Y.; Yamazaki, H.; Kayakiri, N.; Yoshihara, K.; Yatabe, T.; Oku, T. (Fujisawa Pharmaceutical Co., Ltd.); Benzofuran derivs. useful as inhibitors of bone resorption. EP 0757682; JP 1997512795; US 5858995; WO 9529907 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
19273 acetyl chloride 75-36-5 C2H3ClO 详情 详情
(I) 13463 o-Fluoronitrobenzene; 1-fluoro-2-nitrobenzene 1493-27-2 C6H4FNO2 详情 详情
(II) 17791 acetone oxime; Acetoxime 127-06-0 C3H7NO 详情 详情
(III) 25083 acetone O-(2-nitrophenyl)oxime C9H10N2O3 详情 详情
(IV) 25084 2-methyl-7-nitro-1-benzofuran C9H7NO3 详情 详情
(V) 25086 1-(7-amino-2-methyl-1-benzofuran-3-yl)-1-ethanone C11H11NO2 详情 详情
(VI) 24086 benzhydryl 2-[[2-(tert-butoxy)-2-oxoethoxy]imino]-2-[2-(formylamino)-1,3-thiazol-4-yl]acetate C25H25N3O6S 详情 详情
(VII) 25087 2,6-dichlorobenzoyl chloride 4659-45-4 C7H3Cl3O 详情 详情
(VIII) 25088 N-(3-acetyl-2-methyl-1-benzofuran-7-yl)-2,6-dichlorobenzamide C18H13Cl2NO3 详情 详情
Extended Information