HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521660Generated: October 30, 2026
Ammonia → 4-Amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline
https://huagongshe.com/reaction/521660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Chloro-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline | HCID 118205819 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline | HCID 118205828 | — |
Reaction Steps
4.5 ml of a 28% aqueous ammonia solution was added to a mixture of 500 mg of 4-chloro-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline, 8 ml of THF and 5 ml of acetonitrile, and the mixture was stirred at 50° C. for 2 hours. Water was added to the cooled reaction mixture, and the mixture was extracted with t-butyl methyl ether. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 396 mg of 4-amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline (Compound of Present Invention 5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328121B1 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8159266957cd40a3a339e68e78aa5612 |
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| Source note | uspto-grants-2016_05 |
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