HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521669Generated: October 30, 2026
Sodium Thiosulfate → 2-(4-Chloro-2-ethylsulfonylphenyl)-4-ethylamino-7-trifluoromethylquinazoline
https://huagongshe.com/reaction/521669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-(4-Chloro-2-ethylsulfanylphenyl)-4-ethylamino-7-trifluoromethylquinazoline | HCID 118035083 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(4-Chloro-2-ethylsulfonylphenyl)-4-ethylamino-7-trifluoromethylquinazoline | HCID 118035577 | — |
Reaction Steps
375 mg of 3-chloroperbenzoic acid (purity of 65% or more) was added to a mixture of 306 mg of 2-(4-chloro-2-ethylsulfanylphenyl)-4-ethylamino-7-trifluoromethylquinazoline and 5 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 270 mg of 2-(4-chloro-2-ethylsulfonylphenyl)-4-ethylamino-7-trifluoromethylquinazoline (Compound of Present Invention 16).
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-21e281cad50a41b299b852b691175d44 |
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| Source note | uspto-grants-2016_05 |
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