HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Piperidineethanol → HCID 13336380, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Piperidineethanol | HCID 73953 | — |
| Reactant | HCID 20158356 | HCID 20158356 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13336380 | HCID 13336380 | — |
Reaction Steps
Ethyl 2-phenylquinazoline-4-carboxylate (1.7 g) and piperidine-4-ethanol (8 g) are heated at 150° C. for 4 hours. After cooling, water is added and the mixture is extracted with ethyl acetate. The organic phase is dried over magnesium sulphate and evaporated to dryness under reduced pressure. The residue is chromatographed on silica gel with ethyl acetate as the eluant, and the product recovered is recrystallized from isopropyl ether. This gives 1-[(2-phenylquinazolin-4-yl)-carbonyl]-piperidine-4-ethanol (0.5 g), melting at 146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04711890 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-670b5c065a944f6995ddfc6a0c7e14ac |
| Source note | uspto-grants-1987_12 |