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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720915Generated: November 2, 2026

Hydrochloric Acid → HCID 10332165, compound

https://huagongshe.com/reaction/1720915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-PropanolHCID 1031—
ReactantCyanamideHCID 9864—
ReactantHCID 10034899HCID 10034899—
ProductHCID 10332165HCID 1033216544%

Reaction Steps

Into a solution of 3-cyano-5-isopropylaminopyridine (118 mg, 0.73 mmol) in 1-propanol (20 ml) was passed hydrogen chloride gas under ice-cooling for 30 minutes. The reactor was tight sealed, and the mixture was stirred at room temperature for 17 hours. After the reaction was completed, the reaction mixture was concentrated under reduced pressure, and the residue was neutralized with a saturated sodium carbonate solution and extracted with chloroform (50 ml×3). The chloroform layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a yellow syrup. To the syrup was then added an aqueous solution (6 ml) of cyanamide (61 mg, 1.45 mmol), Na2HPO4 (104 mg, 0.73 mmol) and NaH2PO4 ·2H2O (456 mg, 2.92 mmol), and the mixture was stirred at room temperature for 22 hours. After the reaction was completed, the reaction mixture was extracted with chloroform (30 ml×3), and the chloroform layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give propyl N-cyano-5-isopropylamino-3-pyridinecarboximidate (80 mg, 0.33 mmol) as a yellow syrup (Yield 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508293
Source datasetuspto-grants-1996_04
ORD IDord-ea26c595f5764c1bb942f600affb55e8
Source noteuspto-grants-1996_04