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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055118Generated: November 3, 2026

Nicotinic Acid → HCID 178454039, compound

https://huagongshe.com/reaction/2055118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic AcidHCID 938—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178419079HCID 178419079—
SolventDimethylformamideHCID 6228—
ProductHCID 178454039HCID 178454039—

Reaction Steps

10 ml of a N,N-dimethylformamide solution containing 1 g of N-tert-butoxycarbonyl-trans-1,4-cyclohexanediamine, 632 mg of 3-pyridinecarboxylic acid, 1.07 g of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and 757 mg of 1-hydroxybenzotriazole was stirred at room temperature for 24 hours. To the reaction mixture was added an aqueous saturated sodium hydrogencarbonate solution and the resulting mixture was extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was washed with diethyl ether to obtain N-tert-butoxycarbonyl-trans-4-(3-pyridylcarbonylamino)cyclohexylamine. A mixture comprising 1.27 g of this compound and 13 ml of 15% hydrochloric acid-ethanol solution was stirred at 50° C. for 2 hours. After cooling, precipitates were filtered and washed with diethyl ether to obtain 1.12 g of trans-4-(3-pyridylcarbonylamino)cyclohexylamine.dihydrochloride (Reference Example-10-2 in Table 11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332487B2
Source datasetuspto-grants-2008_02
ORD IDord-bc07b6184bba4094b0aadc15721cba04
Source noteuspto-grants-2008_02