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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245359생성일: 2026년 10월 24일

Barbituric Acid → (2r,4s,4As)-8-acetyl-9,10-difluoro-2,4-dimethyl-1,2,4,4a-tetrahydro-2'h,6h-spiro[1,4-oxazino[4,3-a]quinoline-5,5'-pyrimidine]-2',4',6'(1'h,3'h)-trione

https://huagongshe.com/ko/reaction/245359

반응식

참여 물질

역할이름HCID투입량
반응물Barbituric AcidHCID 6211—
반응물5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehydeHCID 58847058—
용매IsopropanolHCID 3776—
생성물(2r,4s,4As)-8-acetyl-9,10-difluoro-2,4-dimethyl-1,2,4,4a-tetrahydro-2'h,6h-spiro[1,4-oxazino[4,3-a]quinoline-5,5'-pyrimidine]-2',4',6'(1'h,3'h)-trioneHCID 58847042—

반응 조건

온도85 °C

반응 단계

To a solution of 5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde (Intermediate 11, 3.0 g, 9.17 mmol) in IPA was added barbituric acid (1.4 g, 11.00 mmol), and the mixture was heated at 85° C. for 12 hours. Solvents were evaporated and the residue was purified over neutral alumina using a gradient of methanol in CH2Cl2 to give the title compound as a racemic mixture in the form of an off-white solid. Yield: 3.0 g (75%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658641B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-3a2ef7a8c82541e096659b691eb6fea3
출처 메모uspto-grants-2014_02