HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329742Generated: November 2, 2026
4-Methylmorpholine → HCID 19871146, compound
https://huagongshe.com/reaction/329742
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 3-Aminoquinuclidine | HCID 123238 | — |
| Reactant | HCID 53899295 | HCID 53899295 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19871146 | HCID 19871146 | — |
Reaction Steps
To a solution of 1.14 g of 3-aminoquinuclidine and 1.0 g of N-methylmorpholine in 30 ml of chloroform is added a solution of 3.8 g of 6-chloro-4-(2,4-dichlorobenzyl)-3,4-dihydro-2-methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid chloride in 20 ml of chloroform under cooling and stirring followed by stirring for 4 hours. The resultant solution is washed with water, aqueous sodium hydrogen carbonate and then water, and dried over magnesium sulfate. After the solvent is distilled off under reduced pressure, the residue is purified with column chromatography using chloroform as an eluent and treated with ethanolic hydrochloric acid to give 6-chloro-4-(2,4-dichlorobenzyl)-3,4-dihydro-2-methyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide hydrochloride monohydrate, melting at 170°-173° 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-9d1fa019346a4a8f82c353bd6ce539dd |
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| Source note | uspto-grants-1990_01 |
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