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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554416Generated: October 30, 2026

Hydrochloric Acid → HCID 66925126, compound

https://huagongshe.com/reaction/554416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantMonomethylamine methanolHCID 57454252—
ReactantHCID 86232889HCID 86232889—
SolventMethanolHCID 887—
ProductHCID 66925126HCID 6692512625%

Reaction Steps

2-Fluoro-5-phenyl-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde (110 mg) was dissolved in methanol (20 mL), 40% methylamine methanol solution (130 mg) was added at room temperature, and the mixture was stirred for 30 min. Sodium borohydride (38 mg) was added at room temperature, and the mixture was stirred for 10 min. 1 mol/L Hydrochloric acid (20 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: hexane-ethyl acetate=3:7→0:1), and dissolved in ethyl acetate (5 mL). A 4 mol/L hydrogen chloride-ethyl acetate solution (1 mL) was added, and the mixture was concentrated under reduced pressure. The residue was crystallized from ethyl acetate to give the title compound as pale-yellow crystals (yield 32 mg, 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-4e84c7ac77184c2696243d52ff85d505
Source noteuspto-grants-2011_11