HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491610Generated: October 31, 2026
1,2-Dichloroethane → HCID 178506230, compound
https://huagongshe.com/reaction/491610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Chloro-4-isothiocyanato-2-(trifluoromethyl)benzene | HCID 520026 | — |
| Reactant | 4-(3,4-Diamino-phenoxy)-pyridine | HCID 17755837 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178506230 | HCID 178506230 | — |
Reaction Steps
To a solution of 4-(pyridin-4-yloxy)-benzene-1,2-diamine (0.273 g, 1.36 mmol) in 20 mL CH3CN was added 1-chloro-4-isothiocyanato-2-trifluoromethyl-benzene (prepared similarly to the procedure described in Preparation III, 0.322 g, 1.36 mmol). The reaction was stirred 18 h at RT. The reaction was diluted with 25 mL CH3CN, and then EDC (0.39 g, 2.03 mmol) was added. The reaction was heated at 80° C. for 2.5 h. The reaction was cooled to RT and concentrated in vacuo. The crude mix was dissolved into EtOAc and water. The layers were separated, and the organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography using a hexane-EtOAc gradient. The partially pure compound was triturated with CH2Cl2 to yield the title compound. MS (MH+)=405.1; Calc'd 404.78 for C19H12ClF3N4O.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07531553B2 |
|---|
| Source dataset | uspto-grants-2009_05 |
|---|
| ORD ID | ord-611cfb898ac04e53a7044f376098c343 |
|---|
| Source note | uspto-grants-2009_05 |
|---|