Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426825Generated: November 2, 2026

1,4-Dioxane hydrochloride → 1-[5-({3-fluoro-2-(2-fluoropyridin-3-yl)-4-[(methylamino)methyl]-1H-pyrrol-1-yl}sulfonyl)-2-furyl]ethanol hydrochloride

https://huagongshe.com/reaction/1426825

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Reactanttert-butyl [(4-fluoro-5-(2-fluoropyridin-3-yl)-1-{[5-(1-hydroxyethyl)-2-furyl]sulfonyl}-1H-pyrrol-3-yl)methyl]methylcarbamateHCID 67397408—
SolventTetrahydrofuranHCID 8028—
Product1-[5-({3-fluoro-2-(2-fluoropyridin-3-yl)-4-[(methylamino)methyl]-1H-pyrrol-1-yl}sulfonyl)-2-furyl]ethanol hydrochlorideHCID 6739691562%

Reaction Steps

To a solution of tert-butyl [(4-fluoro-5-(2-fluoropyridin-3-yl)-1-{[5-(1-hydroxyethyl)-2-furyl]sulfonyl}-1H-pyrrol-3-yl)methyl]methylcarbamate (176 mg) in tetrahydrofuran (2 mL) was added 4 mol/L hydrogen chloride-dioxane solution (3 mL), and the mixture was stirred at room temperature for 6 hr. The reaction mixture was concentrated under reduced pressure, and the residue was recrystallized from a mixed solvent of ethyl acetate-ethanol to give the title compound as a white solid (yield 95.5 mg, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-ec6631c2079d49ed8cb12d2ebe55e919
Source noteuspto-grants-2015_01