Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554439Generated: October 29, 2026

Hydrochloric Acid → HCID 66924815, compound

https://huagongshe.com/reaction/554439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantMonomethylamine methanolHCID 57454252—
ReactantHCID 86620761HCID 86620761—
SolventMethanolHCID 887—
ProductHCID 66924815HCID 6692481571%

Reaction Steps

1-[(3,4-Difluorophenyl)sulfonyl]-5-(pyridin-2-yl)-1H-pyrrole-3-carbaldehyde (100 mg) was dissolved in methanol (20 mL), 40% methylamine methanol solution (112 mg) was added at room temperature, and the mixture was stirred for 30 min. Sodium borohydride (33 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: ethyl acetate), and dissolved in methanol (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 a mixed solvent (1:10) of methanol-tetrahydrofuran to give the title compound as colorless crystals (yield 89 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-1c770d2751f54a5dbcddcffa6fbb9f01
Source noteuspto-grants-2011_11