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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554433Generated: October 30, 2026

Hydrochloric Acid → HCID 66924840, compound

https://huagongshe.com/reaction/554433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantMonomethylamine methanolHCID 57454252—
ReactantHCID 86620785HCID 86620785—
SolventMethanolHCID 887—
ProductHCID 66924840HCID 6692484070%

Reaction Steps

5-(2-Fluorophenyl)-1-[(2-fluorophenyl)sulfonyl]-1H-pyrrole-3-carbaldehyde (330 mg) was dissolved in methanol (33 mL), 40% methylamine methanol solution (370 mg) was added at room temperature, and the mixture was stirred for 30 min. Sodium borohydride (108 mg) was added at room temperature, and the mixture was stirred for 10 min. 1 mol/L Hydrochloric acid (50 mL) was added, and the mixture was stirred for 5 min. The reaction mixture was alkalized with a saturated aqueous sodium hydrogencarbonate solution and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent: ethyl acetate-methanol=1:0→7:3), and dissolved in methanol (5 mL). A 4 mol/L hydrogen chloride-ethyl acetate solution (2 mL) was added, and the mixture was concentrated under reduced pressure. The residue was crystallized from ethyl acetate to give the title compound as colorless crystals (yield 266 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-668d2316c3a446b881084c46920c69b4
Source noteuspto-grants-2011_11