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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 851007생성일: 2026년 10월 24일

Dimethylformamide → 1,4-Dihydro-4-oxo-8-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acid

https://huagongshe.com/ko/reaction/851007

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물ChlorotrimethylsilaneHCID 6397—
반응물L-Pyroglutamic AcidHCID 7405—
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물8-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 12866349—
용매DichloromethaneHCID 6344—
생성물1,4-Dihydro-4-oxo-8-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acidHCID 1313687253.9%

반응 단계

A mixture of 3.87 g (30 mmol) of 5-oxo-L-proline, 2.19 ml (30 mmol) of thionyl chloride, 2.32 ml (30 mmol) of dimethylformamide, and 75 ml of dichloromethane is stirred with cooling for 1 hour. A mixture of 4.08 g (20 mmol) 8-amino-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 8.4 ml (60 mmol) of triethylamine, 7.6 ml (60 mmol) of chlorotrimethylsilane, and 100 ml of dichloromethane is stirred at room temperature for 40 minutes and then is cooled to 0°. The cold acid chloride solution is added to the cold silylated quinoline and the mixture is stirred with cooling for 4 hours and at room temperature overnight. The reaction mixture is evaporated to dryness and the residue is treated with ethanol to give 3.40 g of 1,4-dihydro-4-oxo-8-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04382089
출처 데이터셋uspto-grants-1983_05
ORD IDord-bbb0dffa458949ceaefef443213fc58e
출처 메모uspto-grants-1983_05