Methyl iodide → tert-Butyl (S)-5-(methylsulfanyl)-3,4-dihydro-2H-pyrrole-2-carboxylate
반응식
[S:1]=[C:2]1[NH:6][C@H:5]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:4][CH2:3]1.[CH3:14]I>C1COCC1>[CH3:14][S:1][C:2]1[CH2:3][CH2:4][C@@H:5]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[N:6]=1참가 물질
4
실험 절차
To a solution of thiolactam 1b (10.50 g, 52.2 mmol) in 200 mL THF at rt, was added MeI (13.0 mL, 208.7 mmol). The mixture was stirred for 3.5 h, then concentrated. The residue was partitioned between CH2Cl2 and sat. NaHCO3 and the aqueous phase was extracted with CH2Cl2 (3×). The combined organic extract was dried (Na2SO4) and concentrated to afford 10.17 g (91%) of the title compound, 1c, as a brown oil. 1H NMR (300 MHz, CDCl3) δ4.60 (dd, J=6.2, 7.3, 1H), 2.83-2.58 (m, 2H), 2.49 (s, 3H), 2.37-2.22 (m, 1H), 2.17-2.03 (m, 1H), 1.48 (s, 9H).
후처리
- concentrationconcentrated
- customThe residue was partitioned between CH2Cl2 and sat. NaHCO3
- extractionthe aqueous phase was extracted with CH2Cl2 (3×)
- extractionThe combined organic extract
- dry with materialwas dried (Na2SO4)
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-517d3c7800934dac9b874af78c5cd01d
- 출처 데이터셋
- uspto-grants-2003_11
- 특허 번호
- US06653295B2
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