HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199613Generated: October 29, 2026
1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene → HCID 131735689, compound
https://huagongshe.com/reaction/2199613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene | HCID 2733265 | — |
| Reactant | HCID 125488006 | HCID 125488006 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131735689 | HCID 131735689 | — |
Reaction Steps
To the stirring mixture of 3-(5-aminobenzo[b]thiophen-2-yl)-5-isocyanopyridin-2-amine (1.064 g, 4 mmol, 1 eq) in anhydrous tetrahydrofuran (25 mL) under nitrogen atmosphere was added 4-chloro-3-(trifluoromethyl)phenyl isocyanate (904 mg, 1 eq) and the reaction mixture was stirred at room temperature for three hours. The reaction was then diluted with ethyl acetate, washed sequentially with aqueous ammonium chloride, saturated aqueous sodium bicarbonate, and brine, and dried with anhydrous sodium sulfate. The upper clear solution was decanted and concentrated under reduced pressure to lesser amount, to which was added a small amount of EtOAc-Hex (2:1). Upon a filtration, 1-(2-(2-amino-5-isocyanopyridin-3-yl)benzo[b]thiophen-5-yl)-3-(4-chloro-3-(trifluoromethyl)phenyl)urea was obtained as white solid in the amount of 1.37 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359336B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-14a817e3ae8545818cfbe3a1f83ca387 |
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| Source note | uspto-grants-2016_06 |
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