HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329743Generated: November 2, 2026
4-Methylmorpholine → HCID 19871181, compound
https://huagongshe.com/reaction/329743
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 3-Aminoquinuclidine | HCID 123238 | — |
| Reactant | HCID 54057876 | HCID 54057876 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19871181 | HCID 19871181 | — |
Reaction Steps
To a solution of 1.35 g of 3-aminoquinuclidine and 1.14 g of N-methylmorpholine in 30 ml of chloroform is added a solution of 4.5 g of 6-chloro-4-(3-trifluoromethylbenzyl)-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 recrystallized from ethanol and treated with ethanolic hydrochloric acid to give 6-chloro-4-(3-trifluoromethylbenzyl)-3,4-dihydro-2-methyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide hydrochloride, melting at 271°-274° 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-99e19c1c5abb4a2cb191e3bcfb41afea |
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| Source note | uspto-grants-1990_01 |
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