HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696649Generated: November 1, 2026
Hydrochloric Acid → HCID 178470365, compound
https://huagongshe.com/reaction/1696649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178470375 | HCID 178470375 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178470365 | HCID 178470365 | 73% |
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
| 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-d51c0f8cbc2c4303b6fa4fca9ade3df2 |
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| Source note | uspto-grants-2012_04 |
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