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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060807Generated: November 2, 2026

Hydrochloric Acid → HCID 57504950, compound

https://huagongshe.com/reaction/2060807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 57504952HCID 57504952—
SolventMethanolHCID 887—
ProductHCID 57504950HCID 57504950—

Reaction Conditions

Temperature90 °C

Reaction Steps

N Aqueous hydrochloric acid (8.70 mL) is added to N-((4aS,7aS)-7a-(2,4-difluoro-5-(5-fluoropyridin-3-yl)phenyl)-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-2-yl)benzamide (0.252 g, 0.435 mmol) in methanol (4 mL) and the mixture is heated to 90° C. After 18 hours, the heat is removed and the pH of the reaction mixture is adjusted to basic with 5 N aqueous sodium hydroxide. The mixture is extracted three times with 10% isopropyl alcohol in dichloromethane. The organic layer is concentrated under reduced pressure and the resulting residue is purified by radial chromatography eluting with 3% 2 M ammonia in methanol:dichloromethane to give the title compound as the freebase. The free base is dissolved in minimal dichloromethane and 1 M hydrogen chloride in ether is added in excess. Hexane (1 mL) is added and the solvent is removed under reduced pressure to give the title compound (0.129 g, 67%). ES/MS m/e: 366 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278441B2
Source datasetuspto-grants-2012_10
ORD IDord-a6a707bfc0b44ffda22327500dca3bea
Source noteuspto-grants-2012_10