HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329729Generated: October 26, 2026
Triethylamine → 6-chloro-3,4-dihydro-3-oxo-N-[1-(3-phenoxypropyl)-4-piperidyl]-2H-1,4-benzoxazine-8-carboxamide hydrochloride
https://huagongshe.com/reaction/329729
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 6-Chloro-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carboxylic acid | HCID 14719836 | — |
| Reactant | 1-(3-Phenoxypropyl)piperidin-4-amine | HCID 14802120 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-chloro-3,4-dihydro-3-oxo-N-[1-(3-phenoxypropyl)-4-piperidyl]-2H-1,4-benzoxazine-8-carboxamide hydrochloride | HCID 19871153 | — |
Reaction Steps
A solution of 2.3 g of 6-chloro-3,4-dihydro-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid in 100 ml of tetrahydrofuran is cooled to below 0° C. and 2 ml of triethylamine is added under stirring thereto. Further, 1.1 g of ethyl chlorocarbonate is added and the mixture is stirred for 3 hours. To the resultant mixture is added 2.5 g of 4-amino-1-(3-phenoxypropyl)piperidine and the mixture stirred for 8 hours followed by collecting by filtration and washing with tetrahydrofuran and water. To a suspension of thus obtained crystals in 100 ml of methanol are added 10 ml of 10% hydrochloric acid and 30 ml of water and then the suspension is stirred. The collection of the crystals by filtration gives 6-chloro-3,4-dihydro-3-oxo-N-[1-(3-phenoxypropyl)-4-piperidyl]-2H-1,4 -benzoxazine-8-carboxamide hydrochloride, melting at 290°-300° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04892872 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-fb1a7cbae0144f33855a560d2893804c |
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| Source note | uspto-grants-1990_01 |
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