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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696682Generated: November 1, 2026

Hydrochloric Acid → HCID 178470369, compound

https://huagongshe.com/reaction/1696682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178470377HCID 178470377—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178470369HCID 17847036964%

Reaction Steps

A solution of 6-tert-butyloxy-8-oxo-9-[5-(5-trifluoromethoxy-1H-benzimidazol-2-ylsulfanyl)-furan-2-yl]-2,4,5,7,8,9-hexahydro-pyrrolo[3,4-b][1,7]naphthyridine-3-carboxylic acid ethyl ester (0.65 g, 0.98 mmol) in dioxane (20 ml) is combined with 4N HCl in dioxane (3.57 ml). The reaction mixture is stirred at room temperature for 16 hours. The formed insoluble material is collected by filtration, washed with dioxane (100 ml), pentane (50 ml) and dried under vacuum to yield 350 mg of 8-oxo-9-[5-(5-trifluoromethoxy-1H-benzimidazol-2-ylsulfanyl)-furan-2-yl]-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=64%. Analytical LC/MS (method C): m/z=558 (negative ion mode [M−H]−), m/z=560 (positive ion mode [M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163768B2
Source datasetuspto-grants-2012_04
ORD IDord-28d2feb44bc5453da1c0065613aba72a
Source noteuspto-grants-2012_04