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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070051Generated: November 4, 2026

Butanoyl chloride, 2-oxo- → HCID 16113927, compound

https://huagongshe.com/reaction/2070051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanoyl chloride, 2-oxo-HCID 11007880—
ReactantHCID 16113488HCID 16113488—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16113927HCID 1611392720%

Reaction Conditions

Temperature70 °C

Reaction Steps

1-[4-(4-Fluorophenoxy)-3-trifluoromethyl-phenyl]-3-[4-(1H-pyrazolo[3,4-b]pyridin-4-yloxy)phenyl]urea (50 mg, 0.15 mmol) was dissolved in dichloromethane (5 mL) and THF (3 mL), and ethyloxalyl chloride (70 μL) was added thereto. The resulting mixture was stirred at 70° C. for 3 hours. The reaction solution was concentrated and then purified by reverse-phase HPLC (ODS column, 0.05% TFA-containing water/acetonitrile system, 5% to 95% linear gradient) to give the target compound (9 mg, 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299252B2
Source datasetuspto-grants-2012_10
ORD IDord-3f8c42449f36414a9d4e30578863327c
Source noteuspto-grants-2012_10