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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1289222생성일: 2026년 10월 26일

Dimethyl Sulfoxide → o-Fluoro-p-[N-((6RS)-2-methyl-4-oxo-3-pivaloyloxymethyl-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]benzoic acid

https://huagongshe.com/reaction/1289222

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Calcium CarbonateHCID 10112—
반응물6-bromo-2-methyl-3-pivaloyloxymethyl-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-4-oneHCID 10524601—
반응물p-Amino-o-fluorobenzoic acid 1,1-dimethyl-2-hydroxyethylammonium saltHCID 131720633—
용매WaterHCID 962—
생성물o-Fluoro-p-[N-((6RS)-2-methyl-4-oxo-3-pivaloyloxymethyl-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]benzoic acidHCID 19066365—

반응 단계

A mixture of 6-bromo-2-methyl-3-pivaloyloxymethyl-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-4-one (26 g), p-amino-o-fluorobenzoic acid 1,1-dimethyl-2-hydroxyethylammonium salt (42 g), calcium carbonate (21.4 g) and DMSO (200 ml) was stirred at ambient temperature for 72 hours. The mixture was poured onto a mixture of ice and water (1 liter). The precipitate was isolated, washed with water and dried under vacuum. The product was purified by column chromatography using initially a 9:1 mixture of methylene chloride and methanol and then a 9:1:0.1 mixture of methylene chloride, methanol and acetic acid as eluant. There was thus obtained o-fluoro-p-[N-((6RS)-2-methyl-4-oxo-3-pivaloyloxymethyl-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]benzoic acid as a gum (20 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05747499
출처 데이터셋uspto-grants-1998_05
ORD IDord-569c7e2cab5f4a62929158546ea5e837
출처 메모uspto-grants-1998_05