HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-3-ylmethanol → HCID 13336379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-3-ylmethanol | HCID 107308 | — |
| Reactant | HCID 20158356 | HCID 20158356 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 13336379 | HCID 13336379 | — |
Reaction Steps
The procedure of Example 24 is followed using ethyl 2-phenylquinazoline-4-carboxylate (3 g), piperidine-3-methanol (2.9 g), a 1.6M solution of butyllithium in hexane (31 ml) and tetrahydrofuran (20 ml) as the starting materials. After recrystallisation from ethyl acetate, 1-[(2-phenylquinazolin-4-yl)-carbonyl]-piperidine-3-methanol (1 g), melting at 142° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04711890 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-94fe790f13f842c0b9123dd9549fae72 |
| Source note | uspto-grants-1987_12 |