HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986649Generated: October 30, 2026
HCID 13376462, compound → HCID 13376463, compound
https://huagongshe.com/reaction/986649
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13376462 | HCID 13376462 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13376463 | HCID 13376463 | 66.1% |
Reaction Steps
2.0 g of 2-fluoromethyl-3-(2,4-dimethylphenyl)-6-nitro-4(3H)-quinazolinone are suspended in 35 ml of methanol, and a solution of 5.4 g of stannous chloride dihydrate in 5 ml of conc. hydrochloric acid is added dropwise thereto under ice-cooling and stirring. Then, the mixture is stirred at room temperature overnight. The mixture is concentrated under reduced pressure to remove methanol, and water is added to the residue. The aqueous mixture is neutralized with sodium bicarbonate, and chloroform is added thereto. After stirring the mixture, insoluble materials are filtered off. The chloroform solution is separated from the filtrate and concentrated under reduced pressure to give a crystalline residue. The thus-obtained crystals (1.4 g) are recrystallized from isopropanol. 1.2 g of 2-fluoromethyl-3-(2,4-dimethylphenyl)-6-amino-4(3H)-quinazolinone are obtained as pale yellow prisms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04714702 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-566e4a41ac0449f1b6c34a50087623c3 |
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| Source note | uspto-grants-1987_12 |
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