Methyl bromoacetate → HCID 12914983, 화합물
반응식
[C:1]1([S:7][CH:8]2[NH:11][C:10](=[O:12])[CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[CH2:14][C:15]([O:17][CH3:18])=[O:16]>>[C:1]1([S:7][CH:8]2[N:11]([CH2:14][C:15]([O:17][CH3:18])=[O:16])[C:10](=[O:12])[CH2:9]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1참가 물질
3
실험 절차
Treatment of 4-phenylthioazetidin-2-one (Iwata-Reuyl et. al., J. Nat. Prod., 1993, 56(8), 1373) (8 g) with methyl bromoacetate (7.5 g) under the conditions described for Example 1b gave the title compound as a colourless oil (6 g, 53% yield). 1H NMR δ (CDCl3) 2.87 (1H, dd, H3a), 3.42 (1H, dd, H3b), 3.70 (3H, s, CH3), 3.75, 4.29 (each 1H, d, NCH2), 5.22, (1H, dd, H4), 7.26-7.46 (5H, m, Ph-H).
출처 및 근거
- ORD 기록
- ord-441f47d6b8ff4f7fa4cc5eec1eb286c6
- 출처 데이터셋
- uspto-grants-1999_11
- 특허 번호
- US05990102
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