5-Amino-4-methyl-2-(1-methyl-piperidin-4-yl)-6-nitro-isoindole-1,3-dione → 5,6-Diamino-4-methyl-2-(1-methyl-piperidin-4-yl)-isoindole-1,3-dione

HRID 561907노트

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HRID 561907 반응식
[NH2:1][C:2]1[C:3]([CH3:23])=[C:4]2[C:8](=[CH:9][C:10]=1[N+:11]([O-])=O)[C:7](=[O:14])[N:6]([CH:15]1[CH2:20][CH2:19][N:18]([CH3:21])[CH2:17][CH2:16]1)[C:5]2=[O:22]>[Pd].CO>[NH2:1][C:2]1[C:3]([CH3:23])=[C:4]2[C:8](=[CH:9][C:10]=1[NH2:11])[C:7](=[O:14])[N:6]([CH:15]1[CH2:16][CH2:17][N:18]([CH3:21])[CH2:19][CH2:20]1)[C:5]2=[O:22]

참가 물질

4

실험 절차

To a suspension of 5-Amino-4-methyl-2-(1-methyl-piperidin-4-yl)-6-nitro-isoindole-1,3-dione (1.7 g, 5.34 mmol) and 10% Pd/C (250 mg) was added MeOH (100 mL) carefully and evacuated in vacuo. The flask was filled with hydrogen under balloon pressure and stirred for 1 h. The reaction mixture was filtered and evaporated in vacuo to afford the crude 5,6-diamino-4-methyl-2-(1-methyl-piperidin-4-yl)-isoindole-1,3-dione (1.5 g, quant.), which was used as such for further reaction.

후처리

  1. customevacuated in vacuo
  2. additionThe flask was filled with hydrogen under balloon pressure
  3. filtrationThe reaction mixture was filtered
  4. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-bafe9f1a58624c3197a43437b6b0dad9
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08063225B2

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