HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → Deschloro Loratadine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Azatadine | HCID 19861 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Deschloro Loratadine | HCID 12884174 | — |
Reaction Steps
To a solution of 10.9 g (0.1 mole) of ethylchloroformate in 300 ml of anhydrous benzene is added dropwise, with stirring at room temperature, a solution of 14.5 g (0.05 M) of 11-(N-methyl-4-piperidylidene)-6,11-dihydro-5H-benzo-[5,6]-cyclohepta-[1,2-b]-pyridine (hereinafter referred to as Compound IA) in 200 ml of benzene. The solution is stirred and is heated under reflux overnight (16-20 hrs.). The mixture is cooled and is poured into ice water and the organic layer is separated, washed with water, dried, and then concentrated to dryness. The residue is triturated with petroleum ether and a white solid having a melting point of 106°-107° C. is recrystallized from isopropyl ether after decolorization with decolorizing carbon.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04355036 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-7c279a44c98f414fb0971a8ea9f2cfee |
| Source note | uspto-grants-1982_10 |