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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009056Generated: October 31, 2026

Triethylamine → HCID 42633832, compound

https://huagongshe.com/reaction/1009056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
ReactantHCID 67274431HCID 67274431—
ReactantHCID 86630962HCID 86630962—
SolventAcetonitrileHCID 6342—
ProductHCID 42633832HCID 4263383268%

Reaction Conditions

Temperature60 °C

Reaction Steps

5-(2-Methoxy-ethyl)-4-methyl-thiophene-2-sulfonic acid amide (0.235 g, 1.00 mmol) was dissolved in 6 mL of abs. acetonitrile and treated successively with phenyl chloroformate (0.157 g, 1.00 eq.) and triethylamine (0.348 mL, 2.5 eq.), and the mixture kept at ambient temperature for 1. h. The above prepared 4-ethyl-5-methylsulfanyl-thiazol-2-ylamine (0.211 g, 1.00 eq. as hydrochloride) was then added, and the mixture heated to 60° C. over night. Cooling, pouring onto crashed ice, twofold extraction with ethyl acetate, washing with brine, drying over sodium sulfate, and evaporation of the solvents, followed by flash chromatography (SiO2, ethyl acetate/MeOH=95/5) and trituration over heptane yielded 0.296 g of the title compound as light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973051B2
Source datasetuspto-grants-2011_07
ORD IDord-119f63ccebb6416d9dc9da17a48aedd5
Source noteuspto-grants-2011_07