HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225361Generated: October 25, 2026
Amoxapine → Ethyl 4-(2-Chlorodibenz[b,f][1,4]oxazepin-11-yl)-1-piperazinecarboxylic Acid Ester
https://huagongshe.com/reaction/2225361
Participants
| Role | Name | HCID | Charge |
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| Reactant | Amoxapine | HCID 2170 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-(2-Chlorodibenz[b,f][1,4]oxazepin-11-yl)-1-piperazinecarboxylic Acid Ester | HCID 19004074 | 97% |
Reaction Steps
A mixture of 2.20 g of 2-chloro-11-(1-piperazinyl)dibenz[b,f][1,4]oxazepine, 0.76 g of ethyl chloroformate and 0.97 g of potassium carbonate in 20 ml of N,N-dimethylformamide was stirred at 80° C. for 3 hrs. Ice water was added to the reaction mixture and extracted with ether. The etheral layer was washed with water, dried and concentrated. The residue was chromatographed on silica gel using a mixture of n-hexane and ethyl acetate (1:2) as eluents to give 2.62 g of colorless crystals, which were recrystallized from isopropyl ether to give colorless prisms, mp 121.5°-122.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344828 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-3a7d3ae34f4c4c6cb85cf3f4240a1400 |
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| Source note | uspto-grants-1994_09 |
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