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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099357Generated: November 1, 2026

Acetamidine monohydrochloride → HCID 136388714, compound

https://huagongshe.com/reaction/1099357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 66812423HCID 66812423—
SolventEthanolHCID 702—
ProductHCID 136388714HCID 13638871481.5%

Reaction Conditions

Temperature72.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143424B2
Source datasetuspto-grants-2012_03
ORD IDord-127112c453fe4a09ad0179444cdba0e2
Source noteuspto-grants-2012_03