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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | Calcium Carbonate | HCID 10112 | — |
| 반응물 | 6-bromo-2-methyl-3-pivaloyloxymethyl-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-4-one | HCID 10524601 | — |
| 반응물 | p-Amino-o-fluorobenzoic acid 1,1-dimethyl-2-hydroxyethylammonium salt | HCID 131720633 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 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 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05747499 |
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| 출처 데이터셋 | uspto-grants-1998_05 |
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| ORD ID | ord-569c7e2cab5f4a62929158546ea5e837 |
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| 출처 메모 | uspto-grants-1998_05 |
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