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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 249729생성일: 2026년 10월 25일

N-(4-Ethoxy-5-methylcarbamoylpyridin-2-ylmethyl)-N'-(fluoren-9-ylmethyloxycarbonyl)thiourea → 9H-Fluoren-9-ylmethyl (7-ethoxy-6-methylcarbamoyl-2H-imidazo[1,5-a]pyridin-3-ylidene)carbamate

https://huagongshe.com/reaction/249729

반응식

참여 물질

역할이름HCID투입량
반응물N-(4-Ethoxy-5-methylcarbamoylpyridin-2-ylmethyl)-N'-(fluoren-9-ylmethyloxycarbonyl)thioureaHCID 57791308—
촉매Mercury bis(trifluoroacetate)HCID 2723924—
용매1,4-DioxaneHCID 31275—
생성물9H-Fluoren-9-ylmethyl (7-ethoxy-6-methylcarbamoyl-2H-imidazo[1,5-a]pyridin-3-ylidene)carbamateHCID 178465836—

반응 단계

875 mg of N-(4-ethoxy-5-methylcarbamoyl pyridin-2-ylmethyl)-N′-(fluoren-9-ylmethyloxycarbonyl)thiourea (Example 19a, crude product) were dissolved in 25 ml of dioxane and treated at RT with 837 mg (1.96 mmol) of mercury(II) trifluoroacetate. After 10 minutes, the mixture was concentrated and the residue was taken up in DCM. The organic phase was washed three times with 4% strength LiCl solution and once with water, dried with MgSO4 and concentrated in a rotary evaporator. The crude product thus obtained (590 mg) was reacted further without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863269B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-8b381985904d458e8891b45a0d720ba1
출처 메모uspto-grants-2011_01