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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355601Generated: November 1, 2026

Acetic Acid → HCID 67401550, compound

https://huagongshe.com/reaction/2355601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-Ethoxy-4-methylbenzaldehydeHCID 25242058—
ReactantHCID 67398466HCID 67398466—
SolventEthanolHCID 702—
ProductHCID 67401550HCID 674015503%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2-(piperidin-4-ylamino)-isonicotinonitrile dihydrochloride (43.0 mg, 0.18 mmol, 1.0 equiv; intermediate B15) in ethanol (2 mL), acetic acid (54.1 mg, 0.9 mmol, 5.0 equiv) and triethylamine (36.4 mg, 0.36 mmol, 2.0 equiv) was added 3-ethoxy-4-methyl-benzaldehyde (36.1 mg, 0.22 mmol, 1.2 equiv; intermediate E10) and the mixture stirred at 50° C. After 1 h, sodium cyanoborohydride (13.8 mg, 0.22 mmol, 1.2 equiv), dissolved in ethanol (0.5 mL), was added and the mixture stirred at 50° C. over night. Removal of the solvent under reduced pressure and purification by preparative HPLC on reversed phase eluting with a gradient of acetonitrile/water provided 1.8 mg (3%) of the title compound. MS (ISP): 351.5 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754744B2
Source datasetuspto-grants-2010_07
ORD IDord-40894363138a4e32b988c4a87613fbd0
Source noteuspto-grants-2010_07