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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2248556생성일: 2026년 10월 24일

Dicyclohexylcarbodiimide → 3-pentanone O-{2-chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl]-4-fluorobenzoyl}oxime

https://huagongshe.com/ko/reaction/2248556

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물4-PyrrolidinopyridineHCID 75567—
반응물3-Pentanone oximeHCID 2801745—
반응물2-Chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)pyrimidin-1-yl]benzoic acidHCID 12056789—
용매Diethyl EtherHCID 3283—
생성물3-pentanone O-{2-chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl]-4-fluorobenzoyl}oximeHCID 19994233—

반응 단계

0.9 g of 3-pentanone oxime is added at room temperature to a suspension of 3.0 g of 2-chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl]-4-fluorobenzoic acid in 50 ml of diethyl ether. Thereafter, a solution of 1.9 g of dicyclohexylcarbodiimide and 0.1 g of 4-pyrrolidinopyridine in 15 ml of diethyl ether is added dropwise over 10 minutes. The reaction mixture is stirred at room temperature for 12 hours. Subsequently, it is filtered and evaporated to dryness under reduced pressure. The residue is purified by chromatography on silica gel with n-hexane/diethyl ether (4:1) as the eluent. In this manner there is obtained 3-pentanone O-{2-chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4 -trifluoromethyl-1(2H)-pyrimidinyl]-4-fluorobenzoyl}oxime, m.p. 128°-130° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05041156
출처 데이터셋uspto-grants-1991_08
ORD IDord-e86122d1c61647a2b918633f26b6c004
출처 메모uspto-grants-1991_08