HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-fluoro-6-(1-methoxycarbonyl-2-methyl-2-propenyloxycarbonylamino)-4-propargyl-2H-1,4-benzoxazin-3(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-fluoro-6-isocyanato-4-propargyl-2H-1,4-benzoxazin-3(4H)-one | HCID 11817439 | — |
| Reactant | Methyl 2-hydroxy-3-methylbut-3-enoate | HCID 13461762 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 7-fluoro-6-(1-methoxycarbonyl-2-methyl-2-propenyloxycarbonylamino)-4-propargyl-2H-1,4-benzoxazin-3(4H)-one | HCID 15746685 | — |
Reaction Steps
To a solution of 7-fluoro-6-isocyanato-4-propargyl-2H-1,4-benzoxazin-3(4H)-one (2.5 g) and methyl 2-hydroxy-3-methyl-3-butenoate (1.3 g) in benzene (50 ml), triethylamine (0.5 g) was added at room temperature. The resulting mixture was refluxed for 1 hour, cooled to room temperature, combined with water and extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography using a mixture of toluene and ethyl acetate as the eluent to give Compound No. 72 (2.9 g). nD25.0 1.4868
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05322835 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-f8c194ca2bef4632955007ab3fb3e406 |
| Source note | uspto-grants-1994_06 |