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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916249Generated: October 31, 2026

Triethylamine → HCID 59418316, compound

https://huagongshe.com/reaction/1916249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPropanoyl bromide, 2-bromo-HCID 79047—
Reactant5-Amino-1-(oxan-4-yl)-1H-pyrazole-4-carboxamideHCID 42609131—
SolventDimethylformamideHCID 6228—
ProductHCID 59418316HCID 59418316—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of C2 (5.0 g, 23.8 mmol) and triethylamine (3.65 mL, 26.2 mmol) in anhydrous DMF (50 mL) was cooled in an ice bath and treated drop-wise with 2-bromopropanoyl bromide (5.4 g, 25 mmol). The mixture was stirred at 0° C. for 30 mins, warmed to room temperature and stirred at ambient temperature for an additional 2 h. The reaction was partitioned between EtOAc (200 mL) and aqueous 2N hydrochloric acid (500 mL); the organic phase was washed with saturated aqueous sodium bicarbonate solution (400 mL), saturated aqueous sodium chloride solution (200 mL) and dried over sodium sulfate. Filtration and concentration of the filtrate provided crude C24 as an orange residue, which was used in the next step without purification,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618117B2
Source datasetuspto-grants-2013_12
ORD IDord-2e212b0589eb43cc8fcfff14e4f62105
Source noteuspto-grants-2013_12