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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696678Generated: November 2, 2026

Hydrochloric Acid → HCID 178470360, compound

https://huagongshe.com/reaction/1696678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178470372HCID 178470372—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178470360HCID 17847036095%

Reaction Steps

A solution of 6-tert-butyloxy-9-[5-(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 (0.380 g, 0.64 mmol) in dioxane (20 ml) is combined with 4 N HCl in dioxane (2.32 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 323 mg of 9-[5-(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 orange-brown powder. Yield=95%. Analytical LC/MS method B: m/z=492 (negative ion mode [M−H]−), m/z=494 (positive ion mode [M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163768B2
Source datasetuspto-grants-2012_04
ORD IDord-f665ac8479604c378ddf2f045421a08b
Source noteuspto-grants-2012_04