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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249729Generated: October 25, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Ethoxy-5-methylcarbamoylpyridin-2-ylmethyl)-N'-(fluoren-9-ylmethyloxycarbonyl)thioureaHCID 57791308—
CatalystMercury bis(trifluoroacetate)HCID 2723924—
Solvent1,4-DioxaneHCID 31275—
Product9H-Fluoren-9-ylmethyl (7-ethoxy-6-methylcarbamoyl-2H-imidazo[1,5-a]pyridin-3-ylidene)carbamateHCID 178465836—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863269B2
Source datasetuspto-grants-2011_01
ORD IDord-8b381985904d458e8891b45a0d720ba1
Source noteuspto-grants-2011_01