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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244438Generated: November 3, 2026

Formic Acid → HCID 10227239, compound

https://huagongshe.com/reaction/1244438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 21919395HCID 21919395—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10227239HCID 10227239—

Reaction Conditions

Temperature0 °C

Reaction Steps

Acetic anhydride (0.51 ml) was added directly to formic acid (2.0 ml) which had been cooled to 0° C. and then added a solution of 2-[4-[4-(5-chloropyridin-2-yl)piperazino]sulfonyl-3-(hydroxyamino)butyl]-5-fluoropyrimidine (0.485 g) in tetrahydrofuran (11 ml). The solution was stirred at room temperature for 3 hours and then evaporated in vacuo, the resulting residue was azeotroped with toluene and then it was dissolved in methanol and heated to 40° C. for 30 minutes. The solution was evaporated to dryness and then added diethylether and stirred at room temperature for 10 minutes, solid filtered, dried in vacuo to give N-[1-([4-(5-chloropyridin-2-yl)piperazino]sulfonylmethyl)-3-(5-fluoropyrimidin-2-yl)propyl]-N-hydroxyformamide, (0218 g), mp 154–155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122551B2
Source datasetuspto-grants-2006_10
ORD IDord-dd5360423014474aa65c222ac6c23e23
Source noteuspto-grants-2006_10