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

【结 构 式】

【分子编号】45567

【品名】1-[(1R)-2-(2,4-difluorophenyl)-1-methyl-2-oxoethyl]-3-[4-(1H-1,2,3,4-tetraazol-1-yl)phenyl]-1,3-dihydro-2H-imidazol-2-one

【CA登记号】

【 分 子 式 】C19H14F2N6O2

【 分 子 量 】396.3562064

【元素组成】C 57.58% H 3.56% F 9.59% N 21.2% O 8.07%

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:(XX)

The preparation of the epoxide precursor (XV) can also be carried out by an alternative route starting from the chiral hydroxypropiophenone (XVIII), obtained from ethyl (S)-lactate. Hydroxy ketone (XVIII) was converted to triflate (XIX), which was condensed with the sodium salt of imidazolone (XII), yielding adduct (XX). Addition of (dimethylisopropoxysilyl)methylmagnesium chloride to the propiophenone (XX) furnished carbinol (XIX). Oxidative desilylation of (XIX) with H2O2 in the presence of NaHCO3 afforded diol (XXII). This was converted to the corresponding mesylate (XXIII) and then cyclized to oxirane (XV) in the presence of K2CO3.

2 Itoh, K.; Okonogi, K.; Tasaka, A. (Takeda Chemical Industries, Ltd.); Azole cpds., their production and use. EP 0809640; JP 1997183769; WO 9625410 .
1 Hosono, H.; Itoh, K.; Kitazaki, T.; Ichikawa, T.; Okonogi, K.; Tasaka, A.; Matsushita, Y.; Hayashi, R.; Optically active antifungal azoles. X. Synthesis and antifungal activity of N-[4-(azolyl)phenyl] and N-[4-(azolylmethyl)phenyl]-N'[(1R,2R)-2-(2,4-difluorophenyl)-2-hydroxy-1-methyl-3-(1H,1,2,4-triazol-1-yl)propyl]-azolones. Chem Pharm Bull 2000, 48, 12, 1935.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XII) 45562 1-[4-(1H-1,2,3,4-tetraazol-1-yl)phenyl]-1,3-dihydro-2H-imidazol-2-one C10H8N6O 详情 详情
(XV) 45565 1-[(1R)-1-[(2R)-2-(2,4-difluorophenyl)oxiranyl]ethyl]-3-[4-(1H-1,2,3,4-tetraazol-1-yl)phenyl]-1,3-dihydro-2H-imidazol-2-one C20H16F2N6O2 详情 详情
(XVIII) 45571 (2S)-1-(2,4-difluorophenyl)-2-hydroxy-1-propanone C9H8F2O2 详情 详情
(XIX) 43510 (1S)-2-(2,4-difluorophenyl)-1-methyl-2-oxoethyl trifluoromethanesulfonate C10H7F5O4S 详情 详情
(XIX) 45568 1-[(1R,2S)-2-(2,4-difluorophenyl)-2-hydroxy-3-[isopropoxy(dimethyl)silyl]-1-methylpropyl]-3-[4-(1H-1,2,3,4-tetraazol-1-yl)phenyl]-1,3-dihydro-2H-imidazol-2-one C25H30F2N6O3Si 详情 详情
(XX) 45567 1-[(1R)-2-(2,4-difluorophenyl)-1-methyl-2-oxoethyl]-3-[4-(1H-1,2,3,4-tetraazol-1-yl)phenyl]-1,3-dihydro-2H-imidazol-2-one C19H14F2N6O2 详情 详情
(XXII) 45569 1-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-dihydroxy-1-methylpropyl]-3-[4-(1H-1,2,3,4-tetraazol-1-yl)phenyl]-1,3-dihydro-2H-imidazol-2-one C20H18F2N6O3 详情 详情
(XXIII) 45570 (2S,3R)-2-(2,4-difluorophenyl)-2-hydroxy-3-[2-oxo-3-[4-(1H-1,2,3,4-tetraazol-1-yl)phenyl]-2,3-dihydro-1H-imidazol-1-yl]butyl methanesulfonate C21H20F2N6O5S 详情 详情
Extended Information