HuagongsheHuagongshe Chemistry Print Report · For research reference only
Amoxapine → Ethyl 4-(2-Chlorodibenz[b,f][1,4]oxazepin-11-yl)-1-piperazinepropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Amoxapine | HCID 2170 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-(2-Chlorodibenz[b,f][1,4]oxazepin-11-yl)-1-piperazinepropionate | HCID 19004099 | 88.8% |
Reaction Steps
A mixture of 3.14 g of 2-chloro-11-(1-piperazinyl)dibenz[b,f][1,4]oxazepine and 1.20 g of ethyl acrylate in 16 ml of ethanol was refluxed for 2 hrs. The reaction mixture was concentrated and the residue was chromatographed on silica gel using a mixture of n-hexane and ethyl acetate (2:1 and 1:1) as eluents to give 3.68 g of yellow crystals, which were recrystallized from a mixture of isopropyl ether and n-pentane to give yellow prisms, mp 73°-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05344828 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-4359d8848c7d4e5288d82b7beea1df2c |
| Source note | uspto-grants-1994_09 |