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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1409591생성일: 2026년 10월 25일

(3-methylphenyl)methanesulfonyl Chloride → 5-(benzyloxy)-N,1-dimethyl-6-oxo-2-(m-tolylmethylsulfonamido)-1,6-dihydro-pyrimidine-4-carboxamide

https://huagongshe.com/reaction/1409591

반응식

참여 물질

역할이름HCID투입량
반응물(3-methylphenyl)methanesulfonyl ChlorideHCID 2760662—
반응물Potassium tert-butoxideHCID 23665647—
반응물HCID 86710289HCID 86710289—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물5-(benzyloxy)-N,1-dimethyl-6-oxo-2-(m-tolylmethylsulfonamido)-1,6-dihydro-pyrimidine-4-carboxamideHCID 8671029029.5%

반응 단계

Potassium tert-butoxide (75.9 mg, 676 μmol) was added to a solution of 2-amino-5-(benzyloxy)-N,1-dimethyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide (150 mg, 520 μmol) in THF (15.0 ml) and DMF (3 ml). The resulting mixture was stirred for 10 min and then cooled with an ice-bath. To this mixture was slowly added a solution of (3-methylphenyl)methanesulfonyl chloride (140 mg, 684 μmol) in THF (1 ml). The reaction mixture was stirred at room temperature overnight. A further solution of (3-methylphenyl)methanesulfonyl chloride (140 mg, 684 μmol) in THF (1 ml) was added and then the mixture was stirred at room temperature for 48 hours. The resulting mixture was diluted with EtOAc, washed with saturated NaHCO3 aqueous solution and brine. The organic layers were dried over Na2SO4 and concentrated in vacuo. Flash chromatography (silica gel, 0% to 2% MeOH in DCM) provided the desired product as a light yellow solid (0.070 g; 29%). LCMS: m/z=457 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921388B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-6e6c9378a7ff45c288cd8399662c0aae
출처 메모uspto-grants-2014_12