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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535451생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/535451

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TriphosgeneHCID 94429—
반응물O-AllylhydroxylamineHCID 420841—
반응물Methyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoateHCID 66653263—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물Methyl 5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]-2-{[(prop-2-en-1-yloxy)-carbamoyl]amino}benzoateHCID 86683451160%

반응 단계

0.251 g (0.83 mmol) of triphosgene diluted in 3 ml of dioxane is added, under an inert atmosphere at ambient temperature, to 0.4 g (1.18 mmol) of methyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate in 10 ml of dioxane. After stirring for 2.5 hours, 0.267 g (2.36 mmol) of O-prop-2-en-1-ylhydroxylamine and 0.82 ml (5.91 mmol) of triethylamine are added. The reaction medium is stirred for one hour and then hydrolysed with water. The aqueous phase is extracted with dichloromethane. The organic phase obtained is washed with a 1N aqueous solution of hydrochloric acid and a saturated aqueous solution of sodium chloride, and then dried over sodium sulphate, filtered, and concentrated under reduced pressure. 0.581 g of a yellow solid is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859544B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-5fbf785230f34dc8baeb183daea3150e
출처 메모uspto-grants-2014_10