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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966829Generated: November 1, 2026

Triethylamine → HCID 66732380, compound

https://huagongshe.com/reaction/1966829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 66732657HCID 66732657—
SolventDichloromethaneHCID 6344—
ProductHCID 66732380HCID 6673238066%

Reaction Steps

N-Cyclohexyl-1-ethyl-5-(1-oxa-2,8-diazaspiro[4.5]dec-2-en-3-yl)-1H-pyrazolo[3,4-b]pyridin-4-amine hydrochloride salt (70 mg, 0.00016 mole) (example 22) was taken in dichloromethane (10 ml). Triethyl amine (0.07 ml, 0.00050 mole) and pivaloyl chloride (0.030 ml, 0.00025 mole) were added at 0° C. The reaction mixture was stirred at room temperature overnight. It was diluted with dichloromethane, washed with sodium bicarbonate solution, extracted with brine, dried over anhydrous sodium sulphate and concentrated in vacuo. The crude product obtained was purified by preparative thin layer chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420666B2
Source datasetuspto-grants-2013_04
ORD IDord-7597dacb6a56427ab0f48fe4f89cb790
Source noteuspto-grants-2013_04