HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696682Generated: November 1, 2026
Hydrochloric Acid → HCID 178470369, compound
https://huagongshe.com/reaction/1696682
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178470377 | HCID 178470377 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178470369 | HCID 178470369 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163768B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-28d2feb44bc5453da1c0065613aba72a |
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| Source note | uspto-grants-2012_04 |
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