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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361133Generated: October 30, 2026

Methanol → HCID 45137106, compound

https://huagongshe.com/reaction/1361133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl iodoacetateHCID 12183—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 59278102HCID 59278102—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 45137106HCID 45137106—

Reaction Steps

A solution of 3-[4-({[1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carbonyl]-amino}-methyl)-pyridine-2-sulfonyl]-propionic acid methyl ester (200 mg, 0.4 mmol) in DMSO (5 mL) was treated a 15% solution of sodium methoxide in methanol (150 μL, 0.42 mmol). After 15 minutes, the mixture was cooled (water bath) and ethyl iodoacetate (50 μL, 0.42 mmol) was added followed by removal of the water bath. After 18 hours, the mixture was diluted with EtOAc (30 mL) and water (30 mL) and the organic layer was separated. The aqueous layer was extracted with EtOAc (3×20 mL). The combined organic layers were washed with water (20 mL), dried over magnesium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography using a gradient of 0-6% methanol in dichloromethane. The material from the column was twice triturated with ether, filtered and dried under vacuum to afford the title compound as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879873B2
Source datasetuspto-grants-2011_02
ORD IDord-e2457d3744894f7d9ae26c182fe6e4f0
Source noteuspto-grants-2011_02