HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 54549977, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 8-Chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-5-ol | HCID 14637775 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54549977 | HCID 54549977 | 84.6% |
Reaction Steps
To a mixture of 32.6 mg (0.10 mmole) of 5-hydroxy-8-chloro-11-(4-piperidylidene)-6,11-dihydro-5 H-benzo[5,6]cyclohepta[1,2-b]pyridine and 9.7)l (0.12 mmole) of pyridine in a solution of 2 mL of methanol and 1 mL of CH2Cl2 at 0° C. and under a nitrogen atmosphere was added 11.3) l (0.12 mmole) of acetic anhydride. After 30 min. the mixture was poured into water which was subsequently adjusted to pH of about 9 with aqueous sodium hydroxide. The mixture was extracted 2× with CH2Cl2. The organic portions were combined, washed once with brine, dried over Na2SO4, filtered, and concentrated in vacuo to yield 31.2 mg of the title compound as a glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665726 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-29c07ddea525475990bfdcd6965615ff |
| Source note | uspto-grants-1997_09 |