Hydrochloric Acid → Anthranilamide hydrochloride
Reaction equation
[ClH:1].[C:2]([NH2:11])(=[O:10])[C:3]1[C:4](=[CH:6][CH:7]=[CH:8][CH:9]=1)[NH2:5]>CO>[ClH:1].[C:2]([NH2:11])(=[O:10])[C:3]1[C:4](=[CH:6][CH:7]=[CH:8][CH:9]=1)[NH2:5]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Anthranilamide hydrochloride was prepared by adding 20 ml of concentrated hydrochloric acid (37% by weight) to a solution of 27.3 g of anthranilamide in 200 ml of methanol. This mixture was cooled in an ice bath to precipitate the hydrochloride which was then collected and dried to obtain a product melting at 234°C with decomposition. A 17.4 g (0.1 mole) portion of the hydrochloride obtained above was refluxed for 3 hours with 100 ml acetic anhydride and allowed to stand overnight. The mixture was then cooled in an ice bath and the solids collected by filtration on a Buchner funnel. The filter cake was slurried in 100 ml of water, and warmed to aid solution and then 28% aqueous ammonia was added until the mixture was alkaline. After cooling the 2-methyl-4-(3H)quinazolinone precipitated as a solid, was then collected, washed with a small amount of cold water and dried at 70°C to obtain 6.72 g of the desired product. The 2-methyl-4-(3H)quinazolinone melted at 236°-8°C and was obtained in a 42% yield.
Workup
- temperatureThis mixture was cooled in an ice bath
- customto precipitate the hydrochloride which
- customwas then collected
- customdried
Sources & evidence
- ORD record
- ord-fc474c50faa04c09a9387ed87eab5830
- Source dataset
- uspto-grants-1976_08
- Patent number
- US03973021
Reaction notes
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