HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Piperidin-4-yl)ethan-1-ol → HCID 67340994, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Piperidin-4-yl)ethan-1-ol | HCID 338321 | — |
| Reactant | HCID 86676282 | HCID 86676282 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67340994 | HCID 67340994 | 65% |
Reaction Steps
A mixture of 0.200 g (1.55 mmol) of 1-piperidin-4-yl-ethanol and 0.200 g (0.663 mmol) of 3-chloro-N-(2,5-dichloro-pyridin-3-yl)-benzamide in acetonitrile (10 mL) is heated at 175 C in a microwave reactor for 14 hours. The mixture is cooled to room temperature and concentrated under reduced pressure. The residue is purified by flash silica gel chromatography to give 0.170 g (65.0%) of 3-chloro-N-[5′-chloro-4-(1-hydroxy-ethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-3′-yl]-benzamide as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952004B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-ea4d7f7ac0354d6581df8ee017e4dead |
| Source note | uspto-grants-2015_02 |