HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-(2-amino-5-chloro-3-methylbenzoyl)-N'-methoxycarbonylhydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl carbazate | HCID 80519 | — |
| Reactant | 5-Chloro-3-methyl isatoic anhydride | HCID 11550259 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-amino-5-chloro-3-methylbenzoyl)-N'-methoxycarbonylhydrazine | HCID 66854326 | 60.2% |
Reaction Steps
A mixture of 1.05 g of 6-chloro-8-methyl-1H-benzo[d]-1,3-oxazine-2,4-dione, 0.46 g of methyl carbazate and 20 ml of methanol was heated to reflux for 3 hours. After the reaction mixture was allowed to cool to around room temperature, water was poured thereto and the mixture was extracted with ethyl acetate three times. The resulting organic layer was concentrated under reduced pressure, and the residue was washed with toluene to obtain 0.77 g of N-(2-amino-5-chloro-3-methylbenzoyl)-N′-methoxycarbonylhydrazine of the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968573B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-67b0146654f24a0ebb57468fbf57e13e |
| Source note | uspto-grants-2011_06 |