HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → HCID 178506207, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 4-(Trifluoromethyl)phenyl isothiocyanate | HCID 137134 | — |
| Reactant | 4-(Quinolin-4-yloxy)-benzene-1,2-diamine | HCID 17756493 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178506207 | HCID 178506207 | — |
Reaction Steps
To a solution of 4-(quinolin-4-yloxy)-benzene-1,2-diamine (Step B, 227 mg) in CH3CN (60 mL) was added over 5 min, a solution of 1-isothiocyanato-4-trifluoromethyl-benzene (183 mg) in CH3CN 10 mL). The mixture was stirred for 12 h at RT and EDC (260 mg) was added, followed by CH3CN (30 mL). The resulting mixture was heated at 80° C. for 2 h, then cooled to RT. The solvent was evaporated and the residue was dissolved in EtOAc and washed with water. The organic phase was dried, filtered and evaporated. The residue was purified by flash chromatography in EtOAc to give an orange-brown solid. MS (MH+)=420.9, MW: 420.18 Calc'd for: C23H15F3N4O.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531553B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-e55ed9548e514eb1bda4beff656cd96e |
| Source note | uspto-grants-2009_05 |