HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 66664091, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 66664291 | HCID 66664291 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66664091 | HCID 66664091 | — |
Reaction Steps
Piperidine (1 mL) was added to compound 178 (0.161 g, 0.5 mmol) and the reaction mixture was stirred for 19.5 h. The. reaction mixture was then concentrated under reduced pressure to give a yellow gum. Trituration with 1:4 EtOAc:hexanes gave a small amount of compound 179 (0.041 g). Flash chromatography (1:4 EtOAc:hexanes) of the filtrate gave only a partially separable mixture of the expected products, the acetoxyquinazolinone compound 179 and the hydroxyquinazolinone (total mass 0.122 g). ESI-MS m/z=408 (MH+). The reaction described above and compound 179 are shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08980901B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-1c67eb9a322a49eca19d640b2cc694b4 |
| Source note | uspto-grants-2015_03 |