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HRID 851007作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物ChlorotrimethylsilaneHCID 6397—
反応物L-Pyroglutamic AcidHCID 7405—
反応物TriethylamineHCID 8471—
反応物Thionyl ChlorideHCID 24386—
反応物8-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 12866349—
溶媒DichloromethaneHCID 6344—
生成物1,4-Dihydro-4-oxo-8-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acidHCID 1313687253.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04382089
出典データセットuspto-grants-1983_05
ORD IDord-bbb0dffa458949ceaefef443213fc58e
出典メモuspto-grants-1983_05