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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1356151생성일: 2026년 10월 25일

2-(Benzenesulfonyl)-3-phenyloxaziridine → 2-Amino-4-methanesulfinyl-6-phenoxy-pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/1356151

반응식

참여 물질

역할이름HCID투입량
반응물2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
반응물2-Amino-4-methylsulfanyl-6-phenoxy-pyrimidine-5-carbonitrileHCID 18507391—
용매DichloromethaneHCID 6344—
생성물2-Amino-4-methanesulfinyl-6-phenoxy-pyrimidine-5-carbonitrileHCID 1850734427%

반응 단계

To a stirred suspension of 950 mg (3.68 mmol) 2-amino-4-methylsulfanyl-6-phenoxy-pyrimidine-5-carbonitrile in 20 ml dichloromethane was added 3.84 g (14.7 mmol) 3-phenyl-2-(phenylsulfonyl)oxaziridine and stirring continued for 24 hours at room temperature. The reaction mixture was then concentrated in vacuo and the residue resuspended in ether/hexane and filtered to afford 270 mg (27%) 2-amino-4-methanesulfinyl-6-phenoxy-pyrimidine-5-carbonitrile as a light yellow crystalline solid. ES-MS m/e (%): 275 (M+H+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06586441B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-33282ad0247142cab6529b07968f00c5
출처 메모uspto-grants-2003_07