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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012542Generated: October 26, 2026

Methanol → HCID 16045079, compound

https://huagongshe.com/reaction/1012542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethylamineHCID 6329—
ReactantSodium borohydrideHCID 4311764—
Reactant4-fluoro-5-phenyl-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 86630975—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16045079HCID 1604507939%

Reaction Steps

4-Fluoro-5-phenyl-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehyde (0.27 g) was dissolved in tetrahydrofuran (10 mL), a 2 mol/L solution (0.8 mL) of methylamine in tetrahydrofuran was added, and the mixture was stirred at room temperature for 2 hr. Sodium borohydride (91 mg) and methanol (7 mL) were added, and the mixture was stirred at the same temperature for further 30 min. The reaction mixture was concentrated under reduced pressure. A saturated aqueous sodium hydrogencarbonate solution was added to the residue, and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane-ethyl acetate=19:1→0:1). The above-mentioned operation was repeated to give the title compound (0.22 g, yield 39%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977488B2
Source datasetuspto-grants-2011_07
ORD IDord-84f54f266a9442f38a7f7d9bd22d6390
Source noteuspto-grants-2011_07