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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | 4-Pyrrolidinopyridine | HCID 75567 | — |
| 반응물 | 3-Pentanone oxime | HCID 2801745 | — |
| 반응물 | 2-Chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)pyrimidin-1-yl]benzoic acid | HCID 12056789 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 3-pentanone O-{2-chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl]-4-fluorobenzoyl}oxime | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05041156 |
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| 출처 데이터셋 | uspto-grants-1991_08 |
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| ORD ID | ord-e86122d1c61647a2b918633f26b6c004 |
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| 출처 메모 | uspto-grants-1991_08 |
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