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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696649Generated: November 1, 2026

Hydrochloric Acid → HCID 178470365, compound

https://huagongshe.com/reaction/1696649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178470375HCID 178470375—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178470365HCID 17847036573%

Reaction Steps

A solution of 6-tert-butyloxy-9-[5-(5-hydroxy-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 (0.27 g, 0.46 mmol) in dioxane (20 ml) is combined with 4N HCl in dioxane (1.7 ml). The reaction mixture is stirred at room temperature for 16 hours. The formed insoluble material is collected by filtration, washed with dioxane (50 ml), pentane (20 ml), diisopropylether (20 ml) and dried under vacuum to yield 176 mg of 9-[5-(5-hydroxy-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 white powder. Yield=73%. Analytical L/MS (method C): m/z=490 (negative ion mode [M−H]−), m/z=492 (positive ion mode [M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163768B2
Source datasetuspto-grants-2012_04
ORD IDord-d51c0f8cbc2c4303b6fa4fca9ade3df2
Source noteuspto-grants-2012_04