Carbamate → HCID 21251132, 화합물
반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:14][C:15]([O:17][CH3:18])=[O:16])[CH:5]=[CH:6][C:7]=1[S:8][C:9](=O)N(C)C.C[O-].[Na+].C(=O)([O-])N.C[O-].[Na+].CO.[Br:31][CH2:32][CH2:33]CBr>CO>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:14][C:15]([O:17][CH3:18])=[O:16])[CH:5]=[CH:6][C:7]=1[S:8][CH2:9][CH2:33][CH2:32][Br:31]참가 물질
실험 절차
To a solution of methyl 3-chloro-4-dimethylcarbamoylthiophenylacetate (8.5 g, 0.0295 mol) in methanol (30 mL) was added 25% NaOMe in methanol (7.0 mL, 0.034 mol). The reaction was heated to reflux for 2 h. TLC analysis shows residual starting carbamate. Additional NaOMe/MeOH (1.0 mL) was added and the mixture stirred an additional 30 min at reflux. After cooling to ambient temperature, the thiolate solution was added dropwise to a solution of 1,3-dibromopropane (12 mL, 0.12 mol) in methanol (30 mL). The resulting solution was refluxed for 3 h then cooled to ambient temperature, After standing overnight, the reaction was quenched by pouring into ice water. After adjusting to pH1 with conc. HCl, the aqueous solution was extracted with EtOAc (0.2 L then 2×0.1 L). The combined organics were washed with water, brine, dried over anhyd. MgSO4, filtered, and concentrated. The residue was chromatographed over silica gel with 10% of ethyl acetate in hexane to afford the title compound.
후처리
- temperatureThe reaction was heated
- temperatureto reflux for 2 h
- temperatureat reflux
- temperatureThe resulting solution was refluxed for 3 h
- temperaturethen cooled to ambient temperature
- waitAfter standing overnight
- customthe reaction was quenched
- additionby pouring into ice water
- extractionthe aqueous solution was extracted with EtOAc (0.2 L
- washThe combined organics were washed with water, brine
- customdried over anhyd
- filtrationMgSO4, filtered
- concentrationconcentrated
- customThe residue was chromatographed over silica gel with 10% of ethyl acetate in hexane
출처 및 근거
- ORD 기록
- ord-98c30212f3d144e198e0f6af38cc851d
- 출처 데이터셋
- uspto-grants-2001_03
- 특허 번호
- US06200998B1
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