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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598172Generated: October 30, 2026

Triethylamine → HCID 58938679, compound

https://huagongshe.com/reaction/598172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantCarbonate IonHCID 19660—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58938691HCID 58938691—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58938679HCID 5893867942.2%

Reaction Steps

To 0.14 g (0.29 mmol) of 1-(2,4-dimethylphenyl)-4-(heptan-4-yl)-7-oxo-4,7-dihydro-1H-imidazo[4,5-b]pyridine-6-carboxylic acid in 5 mL of THF was added 0.15 mL (1.1 mmol) of triethylamine and 0.10 mL (1.0 mmol) of ethyl chloroformate. The resulting yellow slurry was stirred at room temperature for 40 min. The crude carbonate solution was then added to 0.135 g (3.6 mmol) of sodium borohydride in 5 mL of ethanol at room temperature and the resulting mixture was stirred for 30 min. The reaction was concentrated in vacuo, diluted with water and extracted with chloroform. The combined extracts were washed with brine, dried over sodium sulfate, filtered and the resulting filtrate was concentrated in vacuo. The crude material thus obtained was purified by flash chromatography eluting with a 3% methanol/dichloromethane mixture to give 45 mg of the title compound as a white solid. Dirty fractions were combined, concentrated and purified to give an additional 23 mg of the title compound. The overall yield of the title compound was 68 mg (65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897607B2
Source datasetuspto-grants-2011_03
ORD IDord-e0e5d4ea58264578982ad5a7ba8f2351
Source noteuspto-grants-2011_03