돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13646생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물Glycine tert-butyl ester hydrochlorideHCID 2725036—
반응물1-Methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acidHCID 12415351—
반응물1-Methyl-2-oxo-1,2-dihydroquinoline-3-carbonyl chlorideHCID 86615891—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 2-(1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetateHCID 6738828427%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728130B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-45ef108b719a4cb788350efe6b0aa700
출처 메모uspto-grants-2010_06