반응식
[CH2:1]([CH:3]1[C:11]2([CH2:16][CH2:15][N:14]([CH3:17])[CH2:13][CH2:12]2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[NH:4]1)[CH3:2].[Cl:18][C:19]1[CH:24]=[CH:23][C:22](F)=[CH:21][CH:20]=1>>[Cl:18][C:19]1[CH:24]=[CH:23][C:22]([N:4]2[C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[C:11]3([CH2:16][CH2:15][N:14]([CH3:17])[CH2:13][CH2:12]3)[CH:3]2[CH2:1][CH3:2])=[CH:21][CH:20]=1참가 물질
3
실험 절차
By following the procedure of Example 1c, 2-ethyl-1'-methylspiro[indoline-3,4'-piperidine], the free base of part a, is treated with 4-chlorofluorobenzene to yield 1-(4-chlorophenyl)-2-ethyl-1'-methylspiro[indoline-3,4'-piperidine].
출처 및 근거
- ORD 기록
- ord-7af89bcb38b1490fa89e70a032408f96
- 출처 데이터셋
- uspto-grants-1982_08
- 특허 번호
- US04345081
연결된 노트
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