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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492896Generated: October 30, 2026

HCID 23153574, compound → HCID 23153066, compound

https://huagongshe.com/reaction/492896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23153574HCID 23153574—
CatalystHCID 178502593HCID 178502593—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23153066HCID 2315306699%

Reaction Steps

4-(2-Fluoro-4-nitrophenoxy)-6-{[4-(1-methylpiperidin-4-yl)piperazin-1-yl]carbonylamino}pyrimidine (145 mg) was dissolved in tetrahydrofuran (20 ml). After adding 20% palladium hydroxide-carbon (100 mg), the mixture was stirred overnight under a hydrogen atmosphere. The catalyst was filtered and washed with tetrahydrofuran. The filtrate and the washings were combined and concentrated under reduced pressure, and the resultant residue was dried under reduced pressure to provide the title compound (134 mg, 99%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-98ea5f6c0e59428089f8ff9947222b78
Source noteuspto-grants-2009_05