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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716195Generated: October 25, 2026

Sodium Carbonate → (S)-3-(1'-Methylcyclohexanecarbonyl)amino-tetrahydropyridin-2-one

https://huagongshe.com/reaction/1716195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Methylcyclohexanecarbonyl chlorideHCID 4189245—
Reactant(3S)-3-Aminopiperidin-2-one--hydrogen chloride (1/1)HCID 45789910—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(S)-3-(1'-Methylcyclohexanecarbonyl)amino-tetrahydropyridin-2-oneHCID 1200315542%

Reaction Steps

(S)-3-Amino-tetrahydropyridin-2-one hydrochloride (2 mmol) and Na2CO3 (6 mmol) in water (25 ml) were added to a solution of 1-methylcyclohexanecarbonyl chloride (2 mmol) in dichloromethane (25 ml) at ambient temperature and the reaction was stirred for 18 hours. The organic layer was then separated and the aqueous phase was extracted with additional dichloromethane. The combined organic layers were dried over Na2SO4 and reduced in vacuo. The residue was purified by silica column chromatography (EtOAc:hexanes 1:3 to MeOH:EtOAc 1:19) to give as an amorphous solid (199 mg, 42%); νmax/cm−1 3335, 3269 (NH), 1650, 1621 (CO), 1529 (NH); δH (500 MHz, CDCl3) 6.65 (1H, br d, J5, NH), 6.59 (1H, br s, NH), 4.18 (1H, dt, J 11.5, 5.5, CHNH), 3.30 (2H, td, J6.5, 2.5, CH2NH), 2.52 (1H, ddt, J 13, 5.5, 4.5, lactam CH2), 1.92-1.83 (4H, m, 2× lactam CH and 2× cyclohexane CH2), 1.55-1.23 (9H, m, lactam CH and 8× cyclohexane CH2) and 1.11 (3H, s, CH3); δC (125 MHz, CDCl3) 178.0, 172.3 (CO), 50.4 (NHCHCO), 42.6 (CH3C quat), 41.5, 35.6, 35.5, 27.0 (CH2), 26.3 (CH3), 25.7, 22.8 (×2), 20.9 (CH2); m/z (MNa+C13H22N2O2Na requires 261.1579) 261.1570.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803794B2
Source datasetuspto-grants-2010_09
ORD IDord-a52a917591094089a6dda17dafaf0093
Source noteuspto-grants-2010_09