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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 507607생성일: 2026년 10월 25일

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 5-(5-Bromo-2-chloropyrimidin-4-yl)-N-methyl-N-phenylthiazol-2-amine

https://huagongshe.com/reaction/507607

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
반응물5-Bromo-2-chloropyrimidineHCID 606665—
반응물2-(N-Methyl-N-phenylamino)thiazoleHCID 23459375—
반응물Sodium AscorbateHCID 23667548—
반응물HCID 178418306HCID 178418306—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물5-(5-Bromo-2-chloropyrimidin-4-yl)-N-methyl-N-phenylthiazol-2-amineHCID 60204505—

반응 조건

온도-78 °C

반응 단계

tBuLi (2.9 mL, 1.1 M solution in pentane, 3.0 mmol) was added to a stirred solution of 0.52 g (2.8 mmol) of 2-(N-Methyl-N-phenylamino)thiazole in 10 mL of Et2O at −78° C. The solution was stirred for 30 min at −78° C. before 0.59 g (3.0 mmol) of 5-bromo-2-chloropyrimidine and 10 mL of THF were added. The reaction solution was stirred for 30 min at −78° C., and then quenched by the addition of 5 mL of AcOH in 15 mL of MeOH. Solid 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (1.4 g, 6.1 mmol) was added and the reaction solution was warmed to 0° C. and stirred for 10 min, then poured into 100 mL of a 0.5 M solution of sodium ascorbate, diluted with 300 mL of water and the crude product removed by filtration and washed repeatedly with water. The residue was azeotroped with toluene and purified by flash chromatography eluting with a linear gradient of 10% EtOAc in hexane to 100% EtOAc to deliver the title compound. MS (M+H)+ 383.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07786132B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-d7ab12fd8d7a446c89821418f978124d
출처 메모uspto-grants-2010_08