HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488803Generated: October 29, 2026
Guanidine Hydrochloride → HCID 178513082, compound
https://huagongshe.com/reaction/488803
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 22267584 | HCID 22267584 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178513082 | HCID 178513082 | 76% |
Reaction Steps
A solution of guanidine hydrochloride (3.11 g, 32.6 mmol) in warm anhydrous ethanol (8 mL) under a nitrogen atmosphere was treated in one portion with sodium methoxide (1.76 g, 32.6 mmol). The resulting slurry was concentrated in vacuo. The residue was treated with anhydrous toluene (10 mL) and concentrated to dryness in vacuo (twice). Each time the vacuum was released to a nitrogen atmosphere. The residue was treated in one portion with ethyl 1-(quinolin-5-yl)-5-cyclopropyl-1H-pyrazole-4-carboxylate (1.00 g, 3.26 mmol) in anhydrous ethanol (8 mL). The resulting mixture was concentrated in vacuo (rotatory evaporator, 80° C. water bath). The residue was treated with anhydrous toluene (10 mL) and the resulting mixture was concentrated in vacuo (three times). The resulting solid was triturated with water (85 mL) and filtered. The solid was air-dried to provide 0.880 g (76% yield) of [1-(quinolin-5-yl)-5-cyclopropyl-1H-pyrazole-4-carbonyl]guanidine dihydrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06974813B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-f962a5f3330041e797bb42b55496d47b |
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| Source note | uspto-grants-2005_12 |
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