HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diiodoethane → HCID 53311312, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diiodoethane | HCID 68980 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | (4-Methyl-pyridin-2-yl)-(6-oxazol-5-yl-pyridin-2-yl)-amine | HCID 53311228 | — |
| Reactant | HCID 53311311 | HCID 53311311 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53311312 | HCID 53311312 | 41% |
Reaction Steps
The 2-iodooxazole derivative was prepared as for [6-(2-chloro-oxazol-5-yl)-pyridin-2-yl]-(4-methyl-pyridin-2-yl)-amine above from (4-methyl-pyridin-2-yl)-(6-oxazol-5-yl-pyridin-2-yl)-amine with LiHMDS (1M solution in THF) and diiodoethane in anhydrous THF to give the title compound as a yellow solid (41%) after purification by column chromatography on SiO2 eluting with 40% EtOAc in cyclohexane. 1H NMR (300 MHz, DMSO-d6) δ=9.81 (s, 1H), 8.10 (d, J=5.0 Hz, 1H), 7.84-7.51 (m, 4H), 7.23 (d, J=7.2 Hz, 1H), 6.77 (d, J=4.6 Hz, 1H), 2.33 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08962665B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-55db21df8a534c34910011a2d7d6c548 |
| Source note | uspto-grants-2015_02 |