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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Piperidinecarboxylic acid | HCID 3773 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4-Dichloro-6-methyl-1,3,5-triazine | HCID 16083 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[4-Methyl-6-(methylamino)-1,3,5-triazin-2-yl]-4-piperidinecarboxylic acid | HCID 59447713 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08008483B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-c8ce9dbea7d94ceab67cc3bd08fd237f |
|---|
| Source note | uspto-grants-2011_08 |
|---|