HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775261Generated: October 29, 2026
Sodium Thiosulfate → 2-(2-Ethylsulfinylphenyl)-4-propylamino-7-trifluoromethylquinazoline
https://huagongshe.com/reaction/1775261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-(2-Ethylsulfanylphenyl)-4-propylamino-7-trifluoromethylquinazoline | HCID 118205827 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(2-Ethylsulfinylphenyl)-4-propylamino-7-trifluoromethylquinazoline | HCID 118205825 | — |
| Product | 2-(2-Ethylsulfonylphenyl)-4-propylamino-7-trifluoromethylquinazoline | HCID 118205836 | — |
Reaction Steps
281 mg of 3-chloroperbenzoic acid (purity of 65% or more) was added to a mixture of 305 mg of 2-(2-ethylsulfanylphenyl)-4-propylamino-7-trifluoromethylquinazoline and 4 ml of chloroform, under ice cooling, and the mixture was stirred at room temperature for 4 hours. A 10% aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution 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 174 mg of 2-(2-ethylsulfinylphenyl)-4-propylamino-7-trifluoromethylquinazoline (Compound of Present Invention 9) and 100 mg of 2-(2-ethylsulfonylphenyl)-4-propylamino-7-trifluoromethylquinazoline (Compound of Present Invention 10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260436B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-dc1f60a94aa44345a78b32c1736676e5 |
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| Source note | uspto-grants-2016_02 |
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