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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453851Generated: November 2, 2026

Oxalyl chloride → HCID 86617820, compound

https://huagongshe.com/reaction/1453851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 68954581HCID 68954581—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 86617820HCID 86617820—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 3-benzyloxy-2-ethoxycarbonyl-5-methyl-4-oxo-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-7-carboxylic acid (250 mg, 0.670 mmol) in anhydrous CH2Cl2 at 0° C. were added 2M oxalyl chloride in CH2Cl2 (1.339 mL, 2.678 mmol) and DMF (1 drop). The reaction was stirred at 0° C. for 30 minutes and allowed to warm to room temperature for 1 hour. The mixture was concentrated in vacuo and azeotroped twice with anhydrous CH2Cl2 to afford the title product. ES MS (M+H)=392.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476666B2
Source datasetuspto-grants-2009_01
ORD IDord-3ac61e66cc5d429a955f7c5826e80e28
Source noteuspto-grants-2009_01