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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275471Generated: November 3, 2026

N,N'-Dicyclohexylurea → 4-Ethylthio-5-methyl-6-(1-ethylpyrazol-5-yl)oxycarbonyl-8-chlorothiochroman

https://huagongshe.com/reaction/1275471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DicyclohexylureaHCID 4277—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-Ethylthio-5-methyl-6-carboxy-8-chlorothiochromanHCID 22118415—
ReactantHCID 178418331HCID 178418331—
Solvent2-Methyl-2-butanolHCID 6405—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product4-Ethylthio-5-methyl-6-(1-ethylpyrazol-5-yl)oxycarbonyl-8-chlorothiochromanHCID 22118393106.9%

Reaction Steps

1.0 Gram (3.3 mmol) of 4-ethylthio-5-methyl-6-carboxy-8-chlorothiochroman was dissolved in 5 ml of t-amyl alcohol, and 0.45 g (4.0 mmol, 1.2 eq.) of 1-ethyl-5-hydroxypyrazole and 0.83 g (4.0 mmol, 1.2 eq.) of N,N'-dicyclohexylcarbodiimide were added. The mixture was stirred at room temperature for 2.5 hours. After the completion of the reaction, ethyl acetate and hexane were added, and liberated N,N'-dicyclohexylurea was filtered off. The filtrate was concentrated and purified by column chromatography (silica gel/hexane+ethyl acetate=5:1) to give 1.4 g (yield 100%) of 4-ethylthio-5-methyl-6-(1-ethylpyrazol-5-yl)oxycarbonyl-8-chlorothiochroman.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159904
Source datasetuspto-grants-2000_12
ORD IDord-705e8cc1da8d4e1f80bef8834a0e5663
Source noteuspto-grants-2000_12