HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912788Generated: November 3, 2026
1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene → HCID 23155264, compound
https://huagongshe.com/reaction/1912788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene | HCID 2733265 | — |
| Reactant | HCID 23155121 | HCID 23155121 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23155264 | HCID 23155264 | 16.4% |
Reaction Steps
In 5 mL of methylene chloride, 37 mg of N-(4-imidazo[4,5-c]pyridin-1-yl-phenyl)hydroxylamine obtained in Step A was dissolved, and 41 mg (1.84 mmol) of 4-chloro-3-(trifluoromethyl)phenyl isocyanate was added thereto and the mixture solution was stirred at room temperature for three hours. The reaction solution was concentrated, and then the residue was partitioned between ethyl acetate and a saturated ammonium chloride aqueous solution. The organic layer was washed with a saturated sodium chloride solution, dried and concentrated under reduced pressure. The residue was triturated with n-hexane:ethyl acetate=1:1 to obtain 12 mg (16%) of 1-(4-chloro-3-(trifluoromethyl)phenyl)-3-hydroxy-3-(4-imidazo-[4,5-c]pyridin-1-ylphenyl)urea (Table 1, Compound No. 45) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08609656B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-c9971faf3b644b118e3fdc9040130bd5 |
|---|
| Source note | uspto-grants-2013_12 |
|---|