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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492883Generated: October 29, 2026

Tetrahydrofuran → HCID 23153122, compound

https://huagongshe.com/reaction/492883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 23153573HCID 23153573—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 23153122HCID 23153122104%

Reaction Steps

After adding tetrahydrofuran (2 ml) and methanol (2 ml) to 4-(2-dimethylaminoethyl)piperazine-1-carboxylic acid [6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-yl]amide (94 mg) under a nitrogen atmosphere, 10% palladium-carbon (46 mg) was added, the atmosphere in the reaction vessel was replaced with hydrogen, and the mixture was stirred for 9 hours. The atmosphere in the reaction vessel was then replaced with nitrogen, and the catalyst was filtered and washed with methanol. The filtrate was concentrated under reduced pressure to provide a crude product of 4-(2-dimethylaminoethyl)piperazine-1-carboxylic acid [6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl]amide (91 mg) as a pale yellow amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-73fae06c27ff4af9ac65e6c649242978
Source noteuspto-grants-2009_05