반응식
[CH2:1]([O:8][C:9](=[O:13])[C@H:10]([CH3:12])[NH2:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.OC1C2N=NNC=2C=CC=1.C1(N=C=NC2CCCCC2)CCCCC1.[CH3:39][O:40][C:41]([CH2:43][CH:44]([CH3:48])[C:45](O)=[O:46])=[O:42].COC(CC(=C)C(O)=O)=O>O1CCOCC1>[CH2:1]([O:8][C:9](=[O:13])[C@H:10]([CH3:12])[NH:11][C:45](=[O:46])[CH:44]([CH3:48])[CH2:43][C:41]([O:40][CH3:39])=[O:42])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
7
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
L-alanine benzyl ester (44.7 g.) and hydroxybenzotriazole (34 g.) are dissolved in dioxane (750 ml.) and the solution is chilled with stirring in an ice-water bath. Dicyclohexylcarbodiimide (51.5 g.) and 3-methoxycarbonyl-2-methylpropanoic acid (36 g.), prepared by hydrogenation of 3-methoxycarbonyl-2-methylene propanoic acid, are added in that order and the mixture is stirred at room temperature for 18 hours. The precipitate is filtered off, and the filtrate is concentrated to dryness in vacuo. The residue is dissolved in ethyl acetate and washed neutral. The ethyl acetate is dried over magnesium sulfate and concentrated to dryness in vacuo to yield N-(3-methoxycarbonyl-2-methylpropanoyl)-L-alanine benzyl ester.
후처리
- temperaturethe solution is chilled
- additionare added in that order
- stirringthe mixture is stirred at room temperature for 18 hours
- filtrationThe precipitate is filtered off
- concentrationthe filtrate is concentrated to dryness in vacuo
- dissolutionThe residue is dissolved in ethyl acetate
- washwashed neutral
- dry with materialThe ethyl acetate is dried over magnesium sulfate
- concentrationconcentrated to dryness in vacuo
출처 및 근거
- ORD 기록
- ord-a30c83f38dab4441a5befde4cfe6999a
- 출처 데이터셋
- uspto-grants-1979_05
- 특허 번호
- US04153725
연결된 노트
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