반응식
Cl.C(N=C=NCCCN(C)C)C.[C:13]1([CH2:19][O:20][C:21]([C:23]2([NH2:29])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]2)=[O:22])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.ON1C2C=CC=CC=2N=N1.[C:40]1([C:49]2[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=2)[CH:45]=[CH:44][C:43]([C:46](O)=[O:47])=[CH:42][CH:41]=1>C(Cl)Cl>[C:13]1([CH2:19][O:20][C:21]([C:23]2([NH:29][C:46]([C:43]3[CH:44]=[CH:45][C:40]([C:49]4[CH:50]=[CH:51][CH:52]=[CH:53][CH:54]=4)=[CH:41][CH:42]=3)=[O:47])[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28]2)=[O:22])[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
2.11 g (11 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added to a solution of 2.33 g (10 mmol) of 1-aminocyclohexanecarboxylic acid phenylmethyl ester, 1.68 g (11 mmol) of 1-hydroxybenzotriazole and 3.23 g (10 mmol) of 4-biphenylcarboxylic acid in 120 ml of methylene chloride under ice-cooling. After the mixture was stirred at room temperature overnight, the reaction solution was concentrated under reduced pressure, ethyl acetate was added thereto, and the mixture was successively washed with water, a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, the residue was purified by silica gel chromatography to obtain 3.51 g (85%) of the title compound.
후처리
- temperaturecooling
- concentrationthe reaction solution was concentrated under reduced pressure, ethyl acetate
- additionwas added
- washthe mixture was successively washed with water
- dry with materialby drying with anhydrous sodium sulfate
- distillationAfter the solvent was distilled off under reduced pressure
- customthe residue was purified by silica gel chromatography
출처 및 근거
- ORD 기록
- ord-357d2c51c7ff4c2e8b3cf31e4b7ed697
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08829209B2
연결된 노트
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