Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352419Generated: October 31, 2026

Oxalyl chloride → HCID 9880843, compound

https://huagongshe.com/reaction/352419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant(3'-Fluoro[1,1'-biphenyl]-4-yl)acetic acidHCID 1393660—
ReactantHCID 22712059HCID 22712059—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9880843HCID 9880843—

Reaction Steps

230 mg of 2-(3′-fluoro-biphenyl-4-yl)-acetic acid is dissolved in 5 ml of tetrahydrofuran, mixed with 0.11 ml of oxalyl chloride and one drop of dimethylformamide, and stirred for 2 hours at room temperature. 62 mg of 1,4,5,6-tetrahydro-cyclopentapyrazol-3-yl-amine is added to this solution. The mixture is stirred for 12 hours at room temperature and then concentrated by evaporation. The residue is extracted with ethyl acetate. The extract is washed with sodium bicarbonate solution and water, dried on magnesium sulfate and concentrated by evaporation. The brown residue is dissolved in 5 ml of methanol and mixed with 0.1 ml of a 30% sodium methylate solution. It is stirred for 4 hours at room temperature and then concentrated by evaporation. The residue is extracted with ethyl acetate. The extract is washed with sodium bicarbonate solution and sodium chloride solution, dried on magnesium sulfate and concentrated by evaporation. A yellow, resinous oil is obtained that is purified by HPLC. 2-(3′-Fluoro-biphenyl-4-yl)-N-(1,4,5,6-tetrahydro-cyclopentapyrazol-3-yl)-acetamide with a melting point of 180-181° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747046B2
Source datasetuspto-grants-2004_06
ORD IDord-87d85bfe71ed464f99d0d5f8ee2c90b3
Source noteuspto-grants-2004_06