HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283261Generated: October 25, 2026
Hydrochloric Acid → Anthranilamide hydrochloride
https://huagongshe.com/reaction/1283261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Anthranilamide | HCID 6942 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Anthranilamide hydrochloride | HCID 23509772 | — |
Reaction Steps
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 allows 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-(3 H)quinazolinone melted at 236°-8°C and was obtained in a 42% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03974277 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-59ecafef273240dd9eb067708e82ebc8 |
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| Source note | uspto-grants-1976_08 |
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