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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678448Generated: October 31, 2026

2,4-Dichloro-6-methyl-1,3,5-triazine → 1-(4-chloro-6-methyl-1,3,5-triazin-2-yl)-N-[(2,4-dichlorophenyl)methyl]-4-piperidinecarboxamide

https://huagongshe.com/reaction/1678448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6-methyl-1,3,5-triazineHCID 16083—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[(2,4-dichlorophenyl)methyl]-4-piperidinecarboxamideHCID 20298096—
SolventAcetonitrileHCID 6342—
Product1-(4-chloro-6-methyl-1,3,5-triazin-2-yl)-N-[(2,4-dichlorophenyl)methyl]-4-piperidinecarboxamideHCID 5944772252%

Reaction Steps

To a 25 mL round-bottomed flask was added 2,4-dichloro-6-methyl-1,3,5-triazine (800 mg, 2.79 mmol) and N-[(2,4-dichlorophenyl)methyl]-4-piperidinecarboxamide (859 mg, 2.79 mmol) in acetonitrile (8.7 mL). Diisopropylethylamine (1.46 mL, 8.36 mmol) was added to give a yellow suspension. The reaction mixture was stirred at room temperature for 15 minutes, at which time LC-MS showed the reaction was complete. This suspension was filtered through a Buchner funnel to afford 1-(4-chloro-6-methyl-1,3,5-triazin-2-yl)-N-[(2,4-dichlorophenyl)methyl]-4-piperidinecarboxamide (596 mg, 1.44 mmol, 52%) as a white solid which was used in the next step without further purification. MS (ES) m/e 416 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008483B2
Source datasetuspto-grants-2011_08
ORD IDord-3d27b8fda95c4f30a1b2c30ce13dcf71
Source noteuspto-grants-2011_08