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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423258Generated: November 1, 2026

Sodium hydride → HCID 178462359, compound

https://huagongshe.com/reaction/2423258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(2R)-2-hydroxypropanimidamide hydrochlorideHCID 42614222—
Reactant5-[2-(1,3-dihydrobenzimidazol-2-ylidene)-3-(3-fluorophenyl)-3-oxopropanoyl]-2-fluorobenzenesulfonyl chlorideHCID 178520872—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178462359HCID 17846235983.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

At room temperature, sodium hydride (579 mg) was added to a THF (70 mL) suspension of (2R)-2-hydroxypropanimidamide hydrochloride (1.65 g), followed by heating up to 60° C. and stirring for 30 minutes. The reaction mixture was cooled to room temperature, and a THF (35 mL) solution of 5-[2-(1,3-dihydro-2H-benzimidazol-2-ylidene)-3-(3-fluorophenyl)-3-oxopropanoyl]-2-fluorobenzenesulfonyl chloride (2.10 g) was added, followed by stirring for 20 minutes. Then, this was subjected to liquid-liquid separation with water and ethyl acetate added thereto, the organic layer was washed with saturated brine, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=50/1) to obtain (2R)-N-({5-[2-(1,3-dihydro-2H-benzimidazol-2-ylidene)-3-(3-fluorophenyl)-3-oxopropanoyl]-2-fluorophenyl}sulfonyl)-2-hydroxypropanimidamide (1.95 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960562B2
Source datasetuspto-grants-2011_06
ORD IDord-4e40bef1d99e486991da5572145d4585
Source noteuspto-grants-2011_06