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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427035Generated: November 2, 2026

Methanol → N-(2-amino-5-chloro-3-methylbenzoyl)-N'-methoxycarbonylhydrazine

https://huagongshe.com/reaction/2427035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl carbazateHCID 80519—
Reactant5-Chloro-3-methyl isatoic anhydrideHCID 11550259—
SolventWaterHCID 962—
ProductN-(2-amino-5-chloro-3-methylbenzoyl)-N'-methoxycarbonylhydrazineHCID 6685432660.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968573B2
Source datasetuspto-grants-2011_06
ORD IDord-67b0146654f24a0ebb57468fbf57e13e
Source noteuspto-grants-2011_06