4-Methylmorpholine → HCID 11647294, 화합물
반응식
[C:1]1([CH2:7][CH2:8][CH2:9][NH2:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CN1CCOCC1.[CH3:18][N:19]([CH3:37])[C:20]1([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][N:32]=2)[CH2:25][CH2:24][C:23]([CH2:27][C:28](O)=[O:29])(O)[CH2:22][CH2:21]1.C1(N=C=NC2CCCCC2)CCCCC1.[OH-].[Na+]>O.CN(C)C=O>[CH3:37][N:19]([CH3:18])[C:20]1([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][N:32]=2)[CH2:25][CH2:24][C:23](=[CH:27][C:28]([NH:10][CH2:9][CH2:8][CH2:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[O:29])[CH2:22][CH2:21]1참가 물질
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- 온도
- 0 °C
실험 절차
3-phenylpropylamine (270 mg, 2.0 mmol) and N-methylmorpholine (0.444 ml, 4.0 mmol) were added to a solution of (4-dimethylamino-1-hydroxy-4-pyridin-2-yl-cyclohexyl)acetic acid (556 mg, 2.0 mmol) in abs. dimethylformamide (30 ml) under argon. The solution was cooled to 0° C., dicyclohexylcarbodiimide (825 mg, 4.0 mmol) was added and the mixture was stirred at RT for 5 d. Working up of the mixture was carried out by separating off the urea which had precipitated out and introducing the filtrate into a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml). Still further urea thereby precipitated out and was separated off. The aqueous phase was diluted with water (300 ml), 5 M sodium hydroxide solution (7 ml, 35 mmol) was added and the mixture was stored at 5° C. for 16 h. The crude product thereby precipitated out as a beige-coloured oily compound (22.8 mg, 30%). After chromatography on silica gel (40 g) with EA/methanol (4:1), the amide was obtained as a beige-coloured oil in a yield of 27% (203 mg).
후처리
- customby separating off the urea which
- customhad precipitated out
- additionintroducing the filtrate
- additioninto a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml)
- customStill further urea thereby precipitated out and
- customwas separated off
- additionwas added
- waitthe mixture was stored at 5° C. for 16 h
- customThe crude product thereby precipitated out as a beige-coloured oily compound (22.8 mg, 30%)
출처 및 근거
- ORD 기록
- ord-e3680564e9bb4874bc59b80348411c04
- 출처 데이터셋
- uspto-grants-2011_09
- 특허 번호
- US08017630B2
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