Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3a,4,5,7a-Tetrahydro-2-benzofuran-1,3-dione | HCID 12726601 | — |
| Reactant | HCID 14347817 | HCID 14347817 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14279665 | HCID 14279665 | 73.5% |
Reaction Steps
6-amino-4-cyanomethyl-7-fluoro-2H-1,4-benzoxazin-3(4H)-one (0.5 g), tetrahydrophthalic anhydride (0.38 g) and acetic acid (10 ml) were mixed with each other, then the mixture was refluxed under heating for 3 hours. After the liquor was allowed to cool, it was added to water (40 ml), and separating crystals were collected by filtration, and then the crystals were dissolved in dichloromethane (30 ml). The dichloromethane solution was washed with a saturated solution of sodium bicarbonate, and water, in that order, and then dehydrated with anhydrous sodium sulfate, and subsequently concentrated. Separated crystals were washed with a small amount of ether to give the desired 2-[4-cyanomethyl-7-fluoro-2H-1,4-benzoxazin-3(4H)-on 6-yl]-4,5,6,7-tetrahydro-2H-isoindole-1,3-dione (0.59 g). mp. 227°-229° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04798620 |
|---|
| Source dataset | uspto-grants-1989_01 |
|---|
| ORD ID | ord-9fa03911a1d5483792a705c41cbef472 |
|---|
| Source note | uspto-grants-1989_01 |
|---|