HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → Y 25130
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 3-Aminoquinuclidine | HCID 123238 | — |
| Reactant | 6-Chloro-4-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carbonyl chloride | HCID 29942006 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Y 25130 | HCID 115000 | — |
Reaction Steps
To a solution of 3.0 g of 3-aminoquinuclidine and 3.0 g of N-methylmorpholine in 60 ml of chloroform is added 6.2 g of 6-chloro-3,4-dihydro-4-methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid chloride under cooling and stirring followed by stirring for 2 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-isopropyl ether and treated with ethanolic hydrochloric acid to give 6-chloro-3,4-dihydro-4-methyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide hydrochloride, melting at 281° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892872 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-3fc083efb68e4fc1b6dec064cc9a1c77 |
| Source note | uspto-grants-1990_01 |