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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615604Generated: October 30, 2026

Ethyl Acetate → HCID 86654953, compound

https://huagongshe.com/reaction/1615604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 67308959HCID 67308959—
SolventMethanolHCID 887—
ProductHCID 86654953HCID 8665495386.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 1-benzyloxycarbonyl-3-[3-(4-methoxycarbonylthiophen-3-yl)-ureido]-5-trifluoromethyl-1H-indole-2-carboxylic acid tert-butyl ester 5G (5.29 g, 8.57 mmol) in anhydrous methanol (50 mL) was added a 0.5 M solution of sodium methoxide (25 mL, 12.5 mmol). The reaction mixture was heated in a microwave reactor at 100° C. for 10 minutes. Ethyl acetate (500 mL) was added and the organic layer was washed with 1 N hydrochloric acid and brine. The organic layer was dried over sodium sulfate. The organic solvent was evaporated under reduced pressure. The crude product was purified by flash column chromatography to provide 3-(2,4-dioxo-1,2-dihydro-4H-thieno[3,4-d]pyrimidin-3-yl)-5-trifluoromethyl-1H-indole-2-carboxylic acid tert-butyl ester 5H (3.36 g, 7.45 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765757B2
Source datasetuspto-grants-2014_07
ORD IDord-8afdcb53a4124413b5ad5bf4a4327721
Source noteuspto-grants-2014_07