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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304916Generated: November 2, 2026

Triethylamine → HCID 178520487, compound

https://huagongshe.com/reaction/2304916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantHOAtHCID 181649—
ReactantHCID 2777277HCID 2777277—
ReactantHCID 178478651HCID 178478651—
SolventHydrochloric AcidHCID 313—
SolventDimethylacetamideHCID 31374—
ProductHCID 178520487HCID 178520487—

Reaction Steps

To a solution of 3-(4-trifluoromethoxyphenyl)acrylic acid (186 mg, 1.0 mmol) in DMA (5 ml), HOAt (136 mg, 1.0 mmol) and DIC (126 mg, 1.0 mmol) were added and the mixture was stirred for 10 min. A mixture prepared from 5-amino-4,5,6,7-tetrahydro-1H-benzimidazole, dihydrochloride (210 mg, 1.0 mmol), DMA (5 ml) and triethylamine (202 mg, 2 mmol) was added to the activated ester and the mixture was stirred for 16 hours at ambient temperature. The volatiles were evaporated and the residue was stirred with a mixture of H2O (40 ml), 1 N hydrochloric acid (20 ml) and diethyl ether (25 ml). The phases were separated and the aqueous phase was washed with diethyl ether (2×25 ml) and then made alkaline to pH 10-11 with 4 N sodium hydroxide. The alkaline mixture was extracted with ethyl acetate (3×50 ml) and the combined organic extracts were dried (magnesium sulphate). The solvent was evaporated in vacuo to give a residue that was dissolved in 1 N hydrochloric acid (50 ml) and the acidic mixture was evaporated to dryness. The residue was re-evaporated with acetone (2×15 ml), stirred with acetone for 1 hour and the solid was isolated by filtration and dried. This afforded 141 mg (36%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437147B1
Source datasetuspto-grants-2002_08
ORD IDord-fe3faed4d0a14fc9be91100dca805e14
Source noteuspto-grants-2002_08