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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914838Generated: November 2, 2026

Phenylacetyl chloride → HCID 58034449, compound

https://huagongshe.com/reaction/1914838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTriethylamineHCID 8471—
Reactantmethyl 7-amino-2-methylpyrazolo[1,5-a]pyrimidine-6-carboxylateHCID 2763438—
SolventDichloromethaneHCID 6344—
ProductHCID 58034449HCID 58034449—

Reaction Conditions

Temperature80 °C

Reaction Steps

A 250 mL round-bottomed flask containing methyl 7-amino-2-methylpyrazolo[1,5-a]pyrimidine-6-carboxylate (1.10 g, 5.0 mmol, 1 eq.), CH2Cl2 (40 mL), and Et3N (2.04 g, 20 mmol, 4 eq.) was added slowly phenylacetyl chloride (6.16 g, 40 mmol, 8 eq.). Then the mixture was heated at 80° C. for 4 h. The mixture was allowed to cool and the solvent was removed in vacuo. The residue was dissolved in CH2Cl2 (40 mL) and water (25 mL). The aqueous phase was extracted with CH2Cl2 (2×15 mL). The combined organic solution was dried over Na2SO4. After filtration and concentration, the residue was purified by silica gel chromatography using MeOH and CH2Cl2 as the mobile phases to furnish Compound (20-1) as a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614221B2
Source datasetuspto-grants-2013_12
ORD IDord-e4319567ddcb4d98bb752bf998e86d7b
Source noteuspto-grants-2013_12