Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 15278638 | HCID 15278638 | — |
| Reactant | Methyl 2-carbamoylcyclohex-1-ene-1-carboxylate | HCID 15334633 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 15278639 | HCID 15278639 | — |
Reaction Steps
First, 0.44 g of N-(7-fluoro-4-propargyl-2H-1,4-benzoxazine-3(4H)-one-6-yl)-acetimidoylchloride and 0.29 g of 3,4,5,6-tetrahydrophthalamic acid monomethyl ester were dissolved in 15 ml of benzene, and 0.17 g of triethylamine was added to the solution at room temperature. After that the stirring was continued for 2 hr at 60° C. After letting the reaction liquid stand to cool the same, it was poured into cool water, and then the organic layer was separated therefrom. The organic layer was washed first with water and then with saturated brine, and then dried by using anhydrous magnesium sulfate. The solvent was concentrated, and then the residue was treated by silica gel column chromatography (development solvent: ethyl acetate/n-hexane) to obtain N-acetyl-N-(7-fluoro-4-propargyl-2H-1,4-benzoxazine-3(4H)-one-6-yl)-3,4,5,6tetrahydrophthalamic acid methyl ester. The melting point was 153°-154° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05468719 |
|---|
| Source dataset | uspto-grants-1995_11 |
|---|
| ORD ID | ord-a5cfd52a4985444cae2a1db220ee2bdd |
|---|
| Source note | uspto-grants-1995_11 |
|---|