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HRID 13646作成日:2026年10月24日

Oxalyl chloride → Tert-butyl 2-(1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetate

https://huagongshe.com/ja/reaction/13646

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物DiisopropylethylamineHCID 81531—
反応物Glycine tert-butyl ester hydrochlorideHCID 2725036—
反応物1-Methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acidHCID 12415351—
反応物1-Methyl-2-oxo-1,2-dihydroquinoline-3-carbonyl chlorideHCID 86615891—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 2-(1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetateHCID 6738828427%

反応手順

1-methyl-2-oxo-1,2-dihydroquinoline-3-carbonyl chloride, prepared from 1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid (Archiv der Pharmazie (1990), 323(2), 67-72) and oxalyl chloride, was added dropwise to a solution of tert-butyl 2-aminoacetate hydrochloride (0.041 g, 0.25 mmol), diisopropylethyl amine (0.086 ml, 0.49 mmol), in dichloromethane (1.00 ml), stirred at room temperature for 1 hr. The reaction mixture was diluted with dichloromethane, washed with water and dried over MgSO4 to afford tert-butyl 2-(1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetate in a 27% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728130B2
出典データセットuspto-grants-2010_06
ORD IDord-45ef108b719a4cb788350efe6b0aa700
出典メモuspto-grants-2010_06