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【结 构 式】

【分子编号】60635

【品名】1-[2-(2,3-dihydro-1H-inden-4-ylamino)-4,5-dihydro-1H-imidazol-1-yl]-1-ethanone

【CA登记号】

【 分 子 式 】C14H17N3O

【 分 子 量 】243.3086

【元素组成】C 69.11% H 7.04% N 17.27% O 6.58%

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)

By reacting 1-acetyl-2-imidazolidinone (VII) with 4-aminoindan (I) and POCl3 at 50 C 1-acetylindanazolidine (VIII) is synthesized, which gives indanazoline by hydrolysis

1 Kirchhoff, T.; Kauff, N.D.; Mitra, N.; et al.; BRCA mutations and risk of prostate cancer in ashkenazi jews. Arzneim-Forsch Drug Res 1980, 30, 9, 1733.
2 May, H.J.; Koening, H. (BASF AG); DE 2652004; FR 2370736; NL 7712149 .
3 Unterhalt, B.; Indanazoline Hydrochloride. Drugs Fut 1981, 6, 7, 417.
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) 60634 2,3-dihydro-1H-inden-4-ylamine; 4-indanamine C9H11N 详情 详情
(VII) 23538 1-acetyl-2-imidazolidinone C5H8N2O2 详情 详情
(VIII) 60635 1-[2-(2,3-dihydro-1H-inden-4-ylamino)-4,5-dihydro-1H-imidazol-1-yl]-1-ethanone C14H17N3O 详情 详情
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