HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696678Generated: November 2, 2026
Hydrochloric Acid → HCID 178470360, compound
https://huagongshe.com/reaction/1696678
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178470372 | HCID 178470372 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178470360 | HCID 178470360 | 95% |
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
| 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-f665ac8479604c378ddf2f045421a08b |
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| Source note | uspto-grants-2012_04 |
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