HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dihydrofuran → N-(4-(3-(2,3-Dihydrofuran-2-YL)pyridin-2-yloxy)phenyl)benzo[D]thiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dihydrofuran | HCID 15570 | — |
| Reactant | N-Methyl dicyclohexylamine | HCID 24210 | — |
| Reactant | N-(4-(3-Iodopyridin-2-yloxy)phenyl)benzo[D]thiazol-2-amine | HCID 59327141 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(4-(3-(2,3-Dihydrofuran-2-YL)pyridin-2-yloxy)phenyl)benzo[D]thiazol-2-amine | HCID 59326959 | — |
Reaction Steps
A mixture of N-(4-(3-iodopyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine (0.403 g, 0.905 mmol), N-methyldicyclohexylamine (0.400 mL, 1.886 mmol, Aldrich), bis(tri-tert-butylphosphine)palladium (0) (0.045 g, 0.088 mmol, Strem) and 2,5-dihydrofuran (0.500 mL, 6.78 mmol, Aldrich) in 5 mL of dioxane was capped under an atmosphere of argon and stirred at rt for 3 h and then heated at 45° C. overnight. The reaction mixture was diluted with MeOH, evaporated onto silica gel and purified by flash chromatography (Isco, (40 gram)) eluting with 2M NH3 in MeOH:CH2Cl2 (0:1→3:97) to give a white amorphous solid. MS (ESI, pos. ion) m/z: 386.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759532B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-f0fe03bd2a96425aac84f25f34cc687c |
| Source note | uspto-grants-2014_06 |