HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700615Generated: November 1, 2026
Hydrochloric Acid → HCID 178428159, compound
https://huagongshe.com/reaction/1700615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 7-(2-Furyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one | HCID 10955297 | — |
| Reactant | HCID 178427660 | HCID 178427660 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178428159 | HCID 178428159 | — |
Reaction Steps
A mixture of 7-(2-furyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one (227 mg), 1-amino-3-hydroxyguanidine p-toluenesulfonate (314 mg) and concentrated hydrochloric acid (0.1 ml) in ethanol (3 ml) was stirred at 90° C. (bath temperature) for 2 hours. The reaction solution was concentrated under reduced pressure, and to the residue were added ethyl acetate (30 ml), tetrahydrofuran (20 ml) and 0.2 N sodium hydroxide (20 ml). The mixture was shaken, and the separated upper layer was washed with 0.2 N sodium hydroxide (10 ml) and water (10 ml, thrice). To the upper layer was added 2 N hydrochloric acid (1 ml), and the mixture was concentrated under reduced pressure. The residue in ethanol (3 ml) was stirred at 90° C. (bath temperature) for 3 hours and cooled, and crystals precipitated while stirring was filtered, washed with ethanol and dried to give 7-(2-furyl)-5-(1-hydroxyguanidin-3-yl)imino-4-methyl-5,6,7,8-tetrahydroquinoline hydrochloride (Compound 97) (154 mg) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350749B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-2ab8f643125245b3893abc2e9dada6f2 |
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| Source note | uspto-grants-2002_02 |
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