HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 67341377, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67340945 | HCID 67340945 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67341377 | HCID 67341377 | 6.6% |
Reaction Steps
A mixture of 0.030 g (0.066 mmol) of N-(4-bromomethyl-5′-chloro-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-3′-yl)-3-chloro-benzamide, 0.028 g (0.033 mmol) of piperidine, and 0.10 mL (0.58 mmol) of N,N-diisopropylethylamine in acetonitrile (1 mL) is heated at 175 C in a microwave reactor for 30 minutes. The mixture is cooled to room temperature and purified by preparative reverse phase HPLC to give 0.001 g (3%) of the title compound (43) as a colorless solid. [M+H]+=461.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952004B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-ee27f1fc215341b6aebae973b12be583 |
| Source note | uspto-grants-2015_02 |