HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857288Generated: November 2, 2026
2-(Methylthio)aniline → HCID 22132716, compound
https://huagongshe.com/reaction/1857288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Methylthio)aniline | HCID 76337 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-[(6,7-Dimethoxyquinolin-4-yl)oxy]aniline | HCID 11594543 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22132716 | HCID 22132716 | 14% |
Reaction Steps
6,7-Dimethoxy-4-(4-aminophenoxy)quinoline (131 mg) was dissolved in toluene (13 ml) with heat, after the addition of triethylamine (2.6 ml), triphosgene (152 mg) was added, and the admixture was refluxed with heat for 2 minutes. 2-Methylthioaniline (0.11 ml) was added to the reaction mixture, and the admixture was refluxed with heat for 10 minutes. After the addition of aqueous sodium hydrogen carbonate, the reaction mixture was extracted 2 times with chloroform, and the organic layer was then washed with brine and dried with anhydrous sodium sulfate. The solvent was removed by reduced-pressure distillation, and the resulting residue was purified by column chromatography on silica gel eluting with chloroform/acetone (4/1) to obtain 29 mg of the title compound (yield: 14%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06143764 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-96b11e4a6f5c45b891e0f7650c3736f6 |
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| Source note | uspto-grants-2000_11 |
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