HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366757Generated: November 2, 2026
1-Chloro-2-isocyanato-4-(trifluoromethyl)benzene → HCID 58451286, compound
https://huagongshe.com/reaction/2366757
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-2-isocyanato-4-(trifluoromethyl)benzene | HCID 2733263 | — |
| 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 58451286 | HCID 58451286 | 78% |
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), 1-chloro-2-isocyanato-4-(trifluoromethyl)benzene (60 μL, 0.40 mmol) was added, and the mixture was stirred at room temperature for 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 (152 mg, 78%) 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-7391bccf58fb4397bfb89a0a267a7b38 |
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| Source note | uspto-grants-2014_04 |
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