HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696675Generated: November 1, 2026
Hydrochloric Acid → HCID 178470363, compound
https://huagongshe.com/reaction/1696675
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178470374 | HCID 178470374 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178470363 | HCID 178470363 | 183.1% |
Reaction Steps
A solution of 6-tert-butyloxy-9-[5-(6-chloro-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 (0.376 g, 0.60 mmol) in dioxane (20 ml) is combined with 4 N HCl in dioxane (2.17 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 310 mg of 9-[5-(6-chloro-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 light brown powder. Yield=92%. Analytical LC/MS (method B): m/z=528 (positive ion mode, [M+H]+, 1 Cl present), m/z=526 (negative ion mode [M−H]−, 1 Cl present)
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-fd4f5f003b9c4073bcd378dcf7a4af99 |
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| Source note | uspto-grants-2012_04 |
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