Dimethylformamide → N-[1-(Cyanomethyl-carbamoyl)-cyclohexyl]-4-(4-methyl-piperazin-1-yl)-benzamide
반응식
[C:1]([CH2:3][NH:4][C:5]([C:7]1([NH2:13])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1)=[O:6])#[N:2].[CH:14]1[CH:15]=[CH:16][C:17]2[N:22](O)N=N[C:18]=2[CH:19]=1.[CH2:24]([N:26]([CH2:29]C)[CH2:27][CH3:28])[CH3:25].CN([CH:34]=[O:35])C>>[C:1]([CH2:3][NH:4][C:5]([C:7]1([NH:13][C:34](=[O:35])[C:14]2[CH:19]=[CH:18][C:17]([N:22]3[CH2:28][CH2:27][N:26]([CH3:29])[CH2:24][CH2:25]3)=[CH:16][CH:15]=2)[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1)=[O:6])#[N:2]참가 물질
5
실험 절차
1-Amino-cyclohexanecarboxylic acid cyanomethyl-amide (1.38 mmol) 4-(4-methyl-piperazin-1-yl)-benzoic acid hydrochloride (1.38 mmol), HOBT (1.38 mmol), WSCD (1.38 mmol) and triethylamine (1.38 mmol) are dissolved in DMF (5 ml) and stirred overnight at rt. After evaporation of the solvent, the residue is dissolved in a mixture of water and sodium carbonate (to ensure slightly basic conditions) and extracted three times with ethyl acetate. The combined extract is dried over sodium sulfate and evaporated. The residue is suspended in diethylether and the solid filtered of and dried (vacuum). A pale powder with mp. 218-220° C., Rf=0.19 (CH2Cl2/MeOH=9:1) is obtained.
후처리
- customAfter evaporation of the solvent
- dissolutionthe residue is dissolved in a mixture of water and sodium carbonate (
- extractionextracted three times with ethyl acetate
- extractionThe combined extract
- dry with materialis dried over sodium sulfate
- customevaporated
- filtrationthe solid filtered of and
- customdried (vacuum)
- customA pale powder with mp. 218-220° C., Rf=0.19 (CH2Cl2/MeOH=9:1) is obtained
출처 및 근거
- ORD 기록
- ord-cbac4d507b4b4d6cafa51a84defb4169
- 출처 데이터셋
- uspto-grants-2003_11
- 특허 번호
- US06642239B2
반응 노트
불러오는 중…