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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 915050생성일: 2026년 10월 24일

Dichloromethane → 6-{6-bromo-5-[(dimethyl-lambda~4~-sulfanylidene)amino]-3-phenyl-2-pyrazinyl}-2-isopropyl-3 (2H)-pyridazinone

https://huagongshe.com/ko/reaction/915050

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물6-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinoneHCID 86600915—
용매AcetoneHCID 180—
용매Dimethyl SulfoxideHCID 679—
생성물6-{6-bromo-5-[(dimethyl-lambda~4~-sulfanylidene)amino]-3-phenyl-2-pyrazinyl}-2-isopropyl-3 (2H)-pyridazinoneHCID 87798659—

반응 조건

온도-55 °C

반응 단계

To a solution of DMSO (0.75 ml) in CH2Cl2 (5 ml) was added trifluoromethanesulfonic anhydride (1.5 ml) dropwise at <−75° C. under nitrogen. A suspension of 6-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinone (3.00 g) in a mixture of DMSO (5 ml) and CH2Cl2 (6 ml) was added and stirred at −65° C. for 2 hours and at −55° C. for one hour. The reaction mixture was quenched with 1N aq. NaOH (20 ml) and stirred at 15° C. for 10 minutes. An organic layer was collected, dried over MgSO4 and concentrated under reduced pressure to give a solid. The solid was suspended in acetone and collected by filtration to give 6-{6-bromo-5-[(dimethyl-lambda˜4˜-sulfanylidene)amino]-3-phenyl-2-pyrazinyl}-2-isopropyl-3(2H)-pyridazinone (3.16 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07265120B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-38ecb570399c4ff8acabdb50667aacbb
출처 메모uspto-grants-2007_09