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

【结 构 式】

【药物名称】FR-190809

【化学名称】N-Cycloheptyl-N-[4-(4-fluorophenoxy)benzyl]-N'-[6-methyl-2,4-bis(methylsulfonyl)pyridin-3-yl]urea

【CA登记号】215589-63-2

【 分 子 式 】C29H34FN3O6S2

【 分 子 量 】603.73723

【开发单位】Fujisawa (Originator)

【药理作用】Lipoprotein Disorders, Treatment of , METABOLIC DRUGS, ACAT Inhibitors

合成路线1

Condensation of 4-bromobenzaldehyde (I) with 4-fluorophenol (II) in the presence of K2CO3 in refluxing dimethylacetamide gave ether (III). Subsequent reductive amination of (III) with cycloheptylamine (IV) using ethanolic NaBH4 afforded secondary amine (V). Phenyl carbamate (VIII) was obtained by treatment of aminopyridine (VI) with phenyl chloroformate (VII) and dimethylaniline. Condensation of this carbamate with amine (V) in the presence of Et3N in refluxing toluene furnished urea (IX) (1). Both sulfide groups of (IX) were finally oxidized to sulfone using meta-chloroperbenzoic acid in CH2Cl2.

1 Tanaka, A.; Terasawa, T.; Hagihara, H.; Ishibe, N.; Sawada, M.; Sakuma, Y.; Hashimoto, M.; Takasugi, H.; Tanaka, H.; Inhibitors of acyl-CoA:cholesterol O-acyltransferase. 3. Discovery of a novel series of N-alkyl-N-[(fluorophenoxy)benzyl]-N'-arylureas with weak toxicological effects on adrenal glands. J Med Chem 1998, 41, 22, 4408.
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) 22231 4-Bromobenzaldehyde 1122-91-4 C7H5BrO 详情 详情
(II) 19639 4-fluorophenol 371-41-5 C6H5FO 详情 详情
(III) 22233 4-(4-fluorophenoxy)benzaldehyde C13H9FO2 详情 详情
(IV) 22234 cycloheptanamine; cycloheptylamine 5452-35-7 C7H15N 详情 详情
(VI) 22235 N-cycloheptyl-N-[4-(4-fluorophenoxy)benzyl]amine; N-[4-(4-fluorophenoxy)benzyl]cycloheptanamine C20H24FNO 详情 详情
(VI) 22239 6-methyl-2,4-bis(methylsulfanyl)-3-pyridinylamine; 6-methyl-2,4-bis(methylsulfanyl)-3-pyridinamine C8H12N2S2 详情 详情
(VII) 13580 1-[(Chlorocarbonyl)oxy]benzene; phenyl chloroformate 1885-14-9 C7H5ClO2 详情 详情
(VIII) 18000 phenyl 6-methyl-2,4-bis(methylsulfanyl)-3-pyridinylcarbamate C15H16N2O2S2 详情 详情
(IX) 22241 N-cycloheptyl-N-[4-(4-fluorophenoxy)benzyl]-N'-[6-methyl-2,4-bis(methylsulfanyl)-3-pyridinyl]urea C29H34FN3O2S2 详情 详情
Extended Information