반응식
[CH3:1][S:2][CH2:3][C@@H:4]([C:9]([OH:11])=O)[NH:5][C:6](=[O:8])[CH3:7].[CH2:12]([N:14](CC)CC)[CH3:13].ClC(OCCCC)=O.C(N)C>O1CCCC1>[CH2:12]([NH:14][C:9](=[O:11])[C@H:4]([CH2:3][S:2][CH3:1])[NH:5][C:6](=[O:8])[CH3:7])[CH3:13]참가 물질
반응 조건
- 온도
- -15 °C
실험 절차
S-Methyl-N-acetyl-L-cysteine (3.54 g, 20 mmole) was dissolved in 25 ml of tetrahydrofuran and 2.8 ml (20 mmole) of triethylamine was added thereto. Upon cooling to -15° C., 2.7 ml (20 mmole) of butyl chloroformate was added dropwise and the mixture was stirred for 20 minutes at that temperature. After cooling to -40° C., 3.0 ml (46.6 mmole) of aqueous 70% ethylamine solution was added in one portion and stirred for 3 hours under ice cooling. The reaction mixture was extracted with 100 ml of ethyl acetate three times and the extracts were washed successively with 2×30 ml of aqueous 5% sodium bicarbonate and 2×30 ml of saturated saline, dried over anhydrous magnesium sulfate and then concentrated in vacuo. The resulting crystals were collected and washed with ethyl ether to give 2.20 g (53.8% yield) of S-methyl-N-acetyl-L-cysteine ethylamide.
후처리
- temperatureAfter cooling to -40° C.
- stirringstirred for 3 hours under ice cooling
- extractionThe reaction mixture was extracted with 100 ml of ethyl acetate three times
- washthe extracts were washed successively with 2×30 ml of aqueous 5% sodium bicarbonate and 2×30 ml of saturated saline
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated in vacuo
- customThe resulting crystals were collected
- washwashed with ethyl ether
출처 및 근거
- ORD 기록
- ord-9801e8cd1afb463dbc6a2df36ec4a580
- 출처 데이터셋
- uspto-grants-1984_04
- 특허 번호
- US04440788
연결된 노트
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