HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181490Generated: November 3, 2026
4-(Trifluoromethyl)benzyl isocyanate → HCID 86598045, compound
https://huagongshe.com/reaction/1181490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Trifluoromethyl)benzyl isocyanate | HCID 22337699 | — |
| Reactant | HCID 69522881 | HCID 69522881 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86598045 | HCID 86598045 | 4% |
Reaction Steps
To a solution of 6-(trifluoromethyl)isoquinolin-5-amine (Description 98; 100 mg, 0.47 mmol) in anhydrous toluene (5 ml) was added [4-(trifluoromethyl)benzyl]isocyanate (Description 58) [0.506M soln in DCM] (1.88 ml; 0.94 mmol) and the mixture heated at reflux overnight. Further [4-(trifluoromethyl)benzyl]isocyanate [0.506M soln in DCM] (1.88 ml; 0.94 mmol) was added and heating continued for 4 days. The toluene was removed, the residue dissolved in methanol (10 ml) and a spatula end of potassium carbonate added. The mixture was then heated at reflux for 15 mins. The mixture was cooled and filtered and the filtrate evaporated. The residue was purified by mass directed HPLC to give the title compound (8 mg, 4%) as a white solid. m/z (ES+) 414 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07285563B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-d75c54c770304ae1bd175a2930fd6d10 |
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| Source note | uspto-grants-2007_10 |
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