Water → HCID 178484611, 화합물
반응식
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([Cl:13])[CH:11]=2)[C:6](=[C:14](OCC)[C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:5]1=[O:24])(=O)C.[CH3:25][N:26]([CH3:38])[C:27]([CH2:29][NH:30][C:31]1[CH:36]=[CH:35][C:34]([NH2:37])=[CH:33][CH:32]=1)=[O:28].O>CN(C)C=O>[CH3:25][N:26]([CH3:38])[C:27]([CH2:29][NH:30][C:31]1[CH:36]=[CH:35][C:34]([NH:37]/[C:14](=[C:6]2\[C:5](=[O:24])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[C:10]([Cl:13])[CH:11]=3)/[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)=[CH:33][CH:32]=1)=[O:28]참가 물질
5
반응 조건
- 온도
- 120 °C
실험 절차
6.0 g of 1-acetyl-3-(1-ethoxy-1-phenylmethylen)-6-chloro-2-indolinone (educt IX) and 3.9 g of N-(dimethylcarbamoylmethyl)-p-phenylenediamine (educt XV.208) are dissolved in 50 ml of dimethylformamide and stirred for 4.5 hours at 120° C. After cooling water is added, the precipitate formed is suction filtered and washed with methanol. The product is purified through a silica gel column with methylene chloride/methanol (100:1) as eluant and finally recrystallised from ether.
후처리
- additionis added
- customthe precipitate formed
- filtrationfiltered
- washwashed with methanol
- customThe product is purified through a silica gel column with methylene chloride/methanol (100:1) as eluant
- customfinally recrystallised from ether
출처 및 근거
- ORD 기록
- ord-8775a0fca40444739f4b7f70e9aeff09
- 출처 데이터셋
- uspto-grants-2009_04
- 특허 번호
- US07514468B2
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