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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504962Generated: November 4, 2026

Toluene → HCID 59135737, compound

https://huagongshe.com/reaction/504962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTributylphosphineHCID 13831—
ReactantEthyl 2-butynoateHCID 78043—
ReactantHCID 57901763HCID 57901763—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59135737HCID 5913573728%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 7-[(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide (4.3 g), ethyl but-2-ynoate (3.2 mL) and tributylphosphine (3.2 mL) in tetrahydrofuran (40 mL)-toluene (40 mL) was stirred at room temperature for 2 days. ethyl but-2-ynoate (1.6 mL) was added to the reaction solution again, and the mixture was stirred at 60° C. for 2 hr. The reaction solution was concentrated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography (ethyl acetate:hexane=2:8-4:6) to give the title compound (1.6 g, yield: 28%) as a pale-brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-46afffb057bc4624aecc1b9f1e063716
Source noteuspto-grants-2010_08