HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389305Generated: October 31, 2026
Acetamidine monohydrochloride → HCID 136388714, compound
https://huagongshe.com/reaction/389305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 66812423 | HCID 66812423 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136388714 | HCID 136388714 | 81.5% |
Reaction Steps
To the solution of 4-[4-(7-Methoxy-6-methyl-indan-4-ylmethyl)-3,5-dimethyl-pyrazol-1-yl]-3-oxo-butyric acid ethyl ester (1.0 gm, 0.0025 mole) in Ethanol (60 ml), Acetamidine hydrochloride (0.71 gm, 0.0075 mole) was added. Further to this, Sodium ethoxide (0.51 gm, 0.0075 mole) was added at 5-10° C. and then stirred at 70-75° C. for 2 hours. The Ethanol was distilled under vacuum and residue was partitioned between Ethyl acetate (100 ml) and water (100 ml). Further aqueous layer was extracted with Ethyl acetate (2×100 ml). The combined volume of Ethyl acetate layer was reduced to 20 ml and then filtered to give 800 mg of desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378118B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-c40e0069ed484298979565de8adc948d |
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| Source note | uspto-grants-2013_02 |
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