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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243215Generated: November 3, 2026

Acetamidine monohydrochloride → HCID 136353895, compound

https://huagongshe.com/reaction/2243215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantHCID 68692078HCID 68692078—
ProductHCID 136353895HCID 136353895—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of N-(4-{[3-(4-cyanotetrahydro-2H-pyran-4-yl)phenyl]thio}phenyl) hydrazinecarboxamide (1.0 g, 2.72 mmol) (example 6) and acetamidine hydrochloride (1.16 g, 12.22 mmol) was evacuated for about 15 minutes. Dry dimethylformamide (10 mL) was added under nitrogen atmosphere and the mixture was heated at about 120° C. for about 7-8 hours. The solvent was evaporated under vacuum and a saturated solution of potassium carbonate was added until the mixture became basic. The resulting mixture was extracted with ethyl acetate, washed with water, dried over anhydrous sodium sulphate, filtered and the solvent evaporated under vacuum to afford a colorless oily residue, which was purified by column chromatography over silica gel using ethyl acetate and hexane (4:1) to yield the title product as a white fluffy solid. Yield: 0.500 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674811B2
Source datasetuspto-grants-2010_03
ORD IDord-3dca2e3cbe264da58447316c6840c0e3
Source noteuspto-grants-2010_03