Triethylamine → 3-{beta-(1-Methylimidazole-4-yl)acryloyl}amino-delta-valerolactam
반응식
C(N(CC)CC)C.O.[OH:9]N1C2C=CC=CC=2N=N1.[CH:19]1([N:25]=[C:26]=[N:27][CH:28]2[CH2:33]C[CH2:31][CH2:30][CH2:29]2)CCCCC1.[NH2:34][CH:35]1[CH2:41][CH2:40][NH:39][C:37](=[O:38])[CH2:36]1.C(=O)(O)[O-].[Na+]>CN(C)C=O>[CH3:19][N:25]1[CH:33]=[C:28]([CH:29]=[CH:30][C:31]([NH:34][CH:35]2[CH2:41][CH2:40][NH:39][C:37](=[O:38])[CH2:36]2)=[O:9])[N:27]=[CH:26]1참가 물질
반응 조건
- 온도
- 80 °C
실험 절차
To a solution of β-(1-methylimidazole-4-yl)acrylrate hydrochloride (7 g, 37.1 mmole) in dimethylformamide (60 ml) was added triethylamine (7.51 g, 74.2 mmole) and 1-hydroxybenzotriazole hydrate (6.25 g, 40.8 mmole) and the mixture was ice-cooled, and then a solution of dicyclohexylcarbodiimide (8.42 g, 40.8 mmole) in dimethylformamide (15 ml) was added dropwise. After stirring at 80° C. for 30 minutes, followed by at room temperature for 30 minutes, 3-amino-δ-valerolactam (5.08 g, 44.5 mmole) was added to the reaction mixture which was heated with stirring for 13 hours. After cooling to room temperature, a sodium bicarbonate solution was added to the mixture which was extracted with a chloroform-methanol mixed solvent. After drying over magnesium sulfate, the solvent was removed under reduced pressure. The residue was subjected to silica gel flash chromatography and then recrystallized from ethanol/chloroform to obtain the titled compound (6.72 g, 73.0%).
후처리
- temperaturecooled
- waitfollowed by at room temperature for 30 minutes
- temperaturewas heated
- stirringwith stirring for 13 hours
- temperatureAfter cooling to room temperature
- extractionwas extracted with a chloroform-methanol mixed solvent
- dry with materialAfter drying over magnesium sulfate
- customthe solvent was removed under reduced pressure
- customrecrystallized from ethanol/chloroform
출처 및 근거
- ORD 기록
- ord-cb67409c2f3945e1b3a66c44315c4520
- 출처 데이터셋
- uspto-grants-1992_10
- 특허 번호
- US05153201
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