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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50382Generated: October 26, 2026

Triethylamine → HCID 18412513, compound

https://huagongshe.com/reaction/50382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantN-Phenyl-beta-alanine methyl esterHCID 89103—
Reactant1H-Thieno[2,3-d]imidazole-5-carboxylic acid, 2-(methoxymethyl)-1-methyl-HCID 18412318—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18412513HCID 18412513—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 0.50 g (2.2 mmol) of 1-methyl-2-methoxymethylthieno[2,3-d]imidazol-5-yl-carboxylic acid in 20 mL of methylene chloride was mixed with 2.0 mL (3.2 g, 27 mmol) of thionyl chloride and refluxed for 60 minutes, during which time the solid gradually dissolved. After distillation of the liquid components, the crude product was taken up twice more in methylene chloride. After the solvent had been eliminated once more, the crude acid chloride was taken up in 20 mL of tetrahydrofuran and added dropwise to a mixture of 0.42 g (2.3 mmol) of N-(2-methoxycarbonylethyl)aniline and 0.92 mL (6.6 mmol) of triethylamine in 30 mL of tetrahydrofuran. After 16 hours stirring at 50° C., the solvent was eliminated and the crude product obtained was purified by chromatography (silica gel; methylene chloride/ethanol=100:1). Yield: 0.66 g (77% of theory); Rf value: 0.47 (silica gel; methylene chloride/ethanol=19:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710055B2
Source datasetuspto-grants-2004_03
ORD IDord-4a77aa06b19c4f5cb74a9aacae018436
Source noteuspto-grants-2004_03