반응식
C(OC1C=CC(N2CCNCC2)=CC=1F)C1C=CC=CC=1.C(Br)CCCCCCC.[F:31][C:32]1[CH:37]=[C:36]([O:38][CH3:39])[C:35]([F:40])=[CH:34][C:33]=1[N:41]1[CH2:46][CH2:45][NH:44][CH2:43][CH2:42]1.[CH:47]1([CH2:53][CH2:54][CH2:55]Cl)[CH2:52][CH2:51][CH2:50][CH2:49][CH2:48]1>>[CH:47]1([CH2:53][CH2:54][CH2:55][N:44]2[CH2:45][CH2:46][N:41]([C:33]3[CH:34]=[C:35]([F:40])[C:36]([O:38][CH3:39])=[CH:37][C:32]=3[F:31])[CH2:42][CH2:43]2)[CH2:52][CH2:51][CH2:50][CH2:49][CH2:48]1참가 물질
5
실험 절차
Production Example 38 was repeated except that 1-(4-benzyloxy-3-fluorophenyl)piperazine and n-octyl bromide were replaced with 1-(2,5-difluoro-4-methoxyphenyl)piperazine (228 mg) and 3-cyclohexylpropyl chloride (161 mg). The resulting crude product was purified on silica gel column chromatography (eluent, ethyl acetate) to provide 1-(3-cyclohexylpropyl)-4-(2,5-difluoro-4-methoxyphenyl)piperazine (342 mg).
후처리
- customThe resulting crude product was purified on silica gel column chromatography (eluent, ethyl acetate)
출처 및 근거
- ORD 기록
- ord-644ec63d6cc74fe2a71d0683d60d8240
- 출처 데이터셋
- uspto-grants-2008_11
- 특허 번호
- US07449466B2
연결된 노트
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