【结 构 式】 |
【分子编号】25953 【品名】2-(3,5-difluorophenyl)-2-cyclopenten-1-one 【CA登记号】 |
【 分 子 式 】C11H8F2O 【 分 子 量 】194.1807264 【元素组成】C 68.04% H 4.15% F 19.57% O 8.24% |
合成路线1
该中间体在本合成路线中的序号:(IV)The bromination of 2-cyclopentenone (I) gives 2-bromocyclopentenone (II), which is condensed with 3,5-difluorophenylboronic acid (III) by means of a Pd catalyst yielding 2-(3,5-difluorophenyl)-2-cyclopentenone (IV). The reaction of (IV) with the aryl lithium (V) affords the cyclopentenol derivative (VI), which is submitted to an oxidation with PDC with simultaneous allylic transposition to give 2-(3,5-difluorophenyl)-3-[4-(methylsulfanyl)phenyl]-2-cyclopenten-1-one (VII). Finally, this compound is oxidized with H 2O2 (Na2WO4) to the target sulfone. The preceding synthetic approach can also be performed with 2-iodo-2-cyclopentenone (obtained by iodination of (I) instead of its bromo analogue (II). The synthetic approaches can also be performed with the arylmagnesium analogue of lithium derivative (V).
【1】 Black, C. (Merck Frosst Canada Inc.); 2-(3,5-Difluorophenyl)-3-(4-(methyl-sulfonyl)phenyl)-2-cyclopenten-1-one useful as an inhibitor of cyclooxygenase-2. EP 0863134; JP 1998251220 . |
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) | 25950 | 2-cyclopenten-1-one | 930-30-3 | C5H6O | 详情 | 详情 |
(II) | 25951 | 2-bromo-2-cyclopenten-1-one | C5H5BrO | 详情 | 详情 | |
(III) | 25952 | 3,5-difluorophenylboronic acid | 156545-07-2 | C6H5BF2O2 | 详情 | 详情 |
(IV) | 25953 | 2-(3,5-difluorophenyl)-2-cyclopenten-1-one | C11H8F2O | 详情 | 详情 | |
(V) | 18808 | [4-(methylsulfanyl)phenyl]lithium | C7H7LiS | 详情 | 详情 | |
(VI) | 25954 | 2-(3,5-difluorophenyl)-1-[4-(methylsulfanyl)phenyl]-2-cyclopenten-1-ol | C18H16F2OS | 详情 | 详情 | |
(VII) | 25955 | 2-(3,5-difluorophenyl)-3-[4-(methylsulfanyl)phenyl]-2-cyclopenten-1-one | C18H14F2OS | 详情 | 详情 |