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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696675Generated: November 1, 2026

Hydrochloric Acid → HCID 178470363, compound

https://huagongshe.com/reaction/1696675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178470374HCID 178470374—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178470363HCID 178470363183.1%

Reaction Steps

A solution of 6-tert-butyloxy-9-[5-(6-chloro-5-fluoro-1H-benzimidazol-2-ylsulfanyl)-furan-2-yl]-8-oxo-2,4,5,7,8,9-hexahydro-pyrrolo[3,4-b]-1,7-naphthyridine-3-carboxylic acid ethyl ester (0.376 g, 0.60 mmol) in dioxane (20 ml) is combined with 4 N HCl in dioxane (2.17 ml) and the mixture is stirred at room temperature for 16 hours. The formed insoluble material is collected by filtration, washed with dioxane (40 ml), pentane (40 ml), diisopropylether (40 ml) and dried under vacuum to yield 310 mg of 9-[5-(6-chloro-5-fluoro-1H-benzimidazol-2-ylsulfanyl)-furan-2-yl]-8-oxo-4,5,6,7,8,9-hexahydro-2H-pyrrolo[3,4-b]-1,7-naphthyridine-3-carboxylic acid ethyl ester hydrochloride as a light brown powder. Yield=92%. Analytical LC/MS (method B): m/z=528 (positive ion mode, [M+H]+, 1 Cl present), m/z=526 (negative ion mode [M−H]−, 1 Cl present)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163768B2
Source datasetuspto-grants-2012_04
ORD IDord-fd4f5f003b9c4073bcd378dcf7a4af99
Source noteuspto-grants-2012_04