Nitroindoline → 2,3-dihydro-1H-indol-1-amine
반응식
[N+:1]([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6][CH2:5]1)([O-])=O>[Pd]>[NH2:1][N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6][CH2:5]1참가 물질
3
실험 절차
Substituted indolines are prepared such as by the procedures described in Scheme 21. Substituted amino-indolines 64 are prepared from the nitroindoline 62 and a ketone in the presence of NaHB(OAc)3 to form the 1-substituted indoline 63. The nitroindoline 63 is hydrogenated, such as with H2 in the presence of a catalyst, such as Pd/C, to yield the amino-indoline 64.
출처 및 근거
- ORD 기록
- ord-485d7b38f6d242e394b7450c812e0fee
- 출처 데이터셋
- uspto-grants-2011_11
- 특허 번호
- US08058445B2
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