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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678404Generated: October 30, 2026

4-Piperidinecarboxylic acid → 1-[4-Methyl-6-(methylamino)-1,3,5-triazin-2-yl]-4-piperidinecarboxylic acid

https://huagongshe.com/reaction/1678404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidinecarboxylic acidHCID 3773—
ReactantMethylamineHCID 6329—
ReactantSodium HydroxideHCID 14798—
Reactant2,4-Dichloro-6-methyl-1,3,5-triazineHCID 16083—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-[4-Methyl-6-(methylamino)-1,3,5-triazin-2-yl]-4-piperidinecarboxylic acidHCID 59447713100%

Reaction Steps

2,4-dichloro-6-methyl-1,3,5-triazine (5 g, 31 mmol) was dissolved in a 1:1 mixture of acetonitrile and water and treated with an aqueous solution of methyl amine (0.88 mL, 31 mmol) at a low temperature maintained by immersing the reaction flask in an ice bath. The pH of the reaction mixture was adjusted to 9-10 with 1M NaOH and the reaction was stirred for 30 minutes. Then, 4-piperidinecarboxylic acid (5 g, 39 mmol) was added and the pH was maintained between 9 and 10 with additions of 1M NaOH as needed. The reaction was allowed to warm to room temperature and stirred for one hour. The reaction mixture was then concentrated and purified by preparative HPLC to provide 1-[4-methyl-6-(methylamino)-1,3,5-triazin-2-yl]-4-piperidinecarboxylic acid (31 mmol, 100%) as a white solid. MS (ES) m/e 252 [M+H]+. 1H NMR (400 MHz, methanol-D4) 4.7 (m, 2H), 3.3 (s, 2H), 3.0 (s, 3H), 2.7 (m, 1H), 2.4 (s, 3H), 2.0 (m, 2H), 1.7 (m, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008483B2
Source datasetuspto-grants-2011_08
ORD IDord-c8ce9dbea7d94ceab67cc3bd08fd237f
Source noteuspto-grants-2011_08