Nitroindoline → 2,3-dihydro-1H-indol-1-amine
反応式
[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]1参加物
3
実験手順
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.
出典と根拠
- ORDレコード
- ord-a2d22edcec944c5bbc04cf379c179a9e
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08642624B2
反応ノート
読み込み中…