3-Fluoropyrrolidine hydrochloride → HCID 178418914, 화합물
반응식
I[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([NH:12][CH:13]=[C:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[NH:16][C:15]2=[O:23])=[CH:8][CH:7]=1.Cl.[F:25][CH:26]1[CH2:30][CH2:29][NH:28][CH2:27]1>>[F:25][CH:26]1[CH2:30][CH2:29][N:28]([CH2:2][CH2:3][CH2:4][O:5][C:6]2[CH:11]=[CH:10][C:9]([NH:12][CH:13]=[C:14]3[C:22]4[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=4)[NH:16][C:15]3=[O:23])=[CH:8][CH:7]=2)[CH2:27]1참가 물질
3
실험 절차
In a manner similar to that described in Example 217, 3-{[4-(3-Iodo-propoxy)-phenylamino]-methylene}-1,3-dihydro-indol-2-one and 3-fluoro-pyrrolidine hydrochloride (226 mg, 1.2 equiv.) (prepared by the method of Giardina, G et al, Synlett (1995), (1), 55–7) are converted to the named compound as a slightly brownish yellow solid (258 mg, 45%).
후처리
- customprepared by the method of Giardina, G et al, Synlett (1995), (1), 55–7)
출처 및 근거
- ORD 기록
- ord-1e3b0e77cbf34e7b9b511e16a9fb45cf
- 출처 데이터셋
- uspto-grants-2006_03
- DOI