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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535442생성일: 2026년 10월 25일

Triethylamine → Methyl 2-({[2-(dimethylamino)-2-oxoethyl]carbamoyl}amino)-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate

https://huagongshe.com/reaction/535442

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TriphosgeneHCID 94429—
반응물2-Amino-N,N-dimethylacetamide acetateHCID 53399009—
반응물Methyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoateHCID 66653263—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물Methyl 2-({[2-(dimethylamino)-2-oxoethyl]carbamoyl}amino)-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoateHCID 66652958143.4%

반응 단계

0.798 g (2.69 mmol) of triphosgene diluted in 10 ml of dioxane is added, under an inert atmosphere at ambient temperature, to 1.3 g (3.84 mmol) of methyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate in 50 ml of dioxane. After stirring for 1 hour, 1.25 g (7.68 mmol) of N,N-dimethylglycinamide acetate and 2.68 ml (19.21 mmol) of triethylamine are added. The reaction medium is stirred overnight at ambient temperature and then hydrolysed with water. The aqueous phase is extracted with dichloromethane. The organic phase obtained is dried over sodium sulphate, filtered, and then concentrated under reduced pressure. 1.8 g of a yellow solid are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859544B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-7fe39e2e149f470199cb02595e447c39
출처 메모uspto-grants-2014_10