Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581560Generated: November 2, 2026

Propargyl alcohol → HCID 178522931, compound

https://huagongshe.com/reaction/1581560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178522930HCID 178522930—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductHCID 178522931HCID 178522931—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2-bromo-N-(4-chlorobenzyl)-8-hydroxypyrido[3,2-d]pyrimidine-7-carboxamide (Preparation 6, 1.97 g), (Ph3P)2PdCl2 (175 mg), and triethylamine (5.0 mL) in DMF (50 mL) is heated to 90° C. Propargyl alcohol (2.5 mL) is slowly added to the mixture over 20 h. The reaction mixture is allowed to cool to room temperature, poured into saturated aqueous NH4Cl solution (200 mL), and extracted with ethyl acetate (3×100 mL). The combined organic layers are dried (MgSO4) and concentrated. The crude product is purified by column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730682B2
Source datasetuspto-grants-2004_05
ORD IDord-210fc15bc064469f880c4796cf18c38c
Source noteuspto-grants-2004_05