HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366758Generated: November 2, 2026
2-Chloro-4-(trifluoromethyl)phenyl isocyanate → HCID 86657960, compound
https://huagongshe.com/reaction/2366758
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-4-(trifluoromethyl)phenyl isocyanate | HCID 5102533 | — |
| Reactant | N-{5-[(3-amino-4-fluorophenyl)(methyl)amino][1,3]thiazolo[5,4-b]pyridin-2-yl}cyclopropanecarboxamide | HCID 86646059 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86657960 | HCID 86657960 | 64% |
Reaction Steps
N-{5-[(3-Amino-4-fluorophenyl)(methyl)amino][1,3]thiazolo[5,4-b]pyridin-2-yl}cyclopropanecarboxamide (120 mg, 0.34 mmol) produced in Example 1(x) was dissolved in N,N-dimethylformamide (1.5 mL), 2-chloro-1-isocyanato-4-(trifluoromethyl)benzene (62 μL, 0.40 mmol) was added, and the mixture was stirred at room temperature 6 hr. The reaction mixture was diluted with ethyl acetate (10 mL), and washed successively with saturated aqueous sodium hydrogen carbonate solution (10 mL) and saturated brine (10 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate/hexane=50/50→100/0), and the obtained solution was concentrated under reduced pressure. The residue was recrystallized from ethyl acetate to give the title compound (125 mg, 64%) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697874B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-a6795b82ad7640b0a85f055aeef415f3 |
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| Source note | uspto-grants-2014_04 |
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