HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloro-6-methyl-1,3,5-triazine | HCID 16083 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-[(2,4-dichlorophenyl)methyl]-4-piperidinecarboxamide | HCID 20298096 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(4-chloro-6-methyl-1,3,5-triazin-2-yl)-N-[(2,4-dichlorophenyl)methyl]-4-piperidinecarboxamide | HCID 59447722 | 52% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08008483B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-3d27b8fda95c4f30a1b2c30ce13dcf71 |
| Source note | uspto-grants-2011_08 |