HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloropyrimidine → N-(1-pyridin-4-ylethyl)formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86599800 | HCID 86599800 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(1-pyridin-4-ylethyl)formamide | HCID 2771720 | — |
Reaction Steps
N-(1-Piperidin-4-yl-ethyl)-formamide; compound with acetic acid (350 mg, 1.61 mmol), 2,4-dichloro-pyrimidine (265 mg, 1.78 mmol) and ethyl-diisopropyl-amine (848 mg, 6.56 mmol) in 20 ml of ethanol were heated under reflux for 5 hours. The mixture was evaporated and the residue dissolved in water and extracted with ethyl acetate. The organic layer was dried with MgSO4 and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06953857B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-35dac77553444a7fa1206542e86ca4d8 |
| Source note | uspto-grants-2005_10 |