HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 7-[2-(2,2,2-Trifluoro-ethyl)-2h-tetrazol-5-yl]-imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 2,2,2-Trifluoroethyl trifluoromethanesulfonate | HCID 80366 | — |
| Reactant | 7-(2H-Tetrazol-5-yl)-imidazo[1,2-a]pyridine | HCID 59277761 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-[2-(2,2,2-Trifluoro-ethyl)-2h-tetrazol-5-yl]-imidazo[1,2-a]pyridine | HCID 59321162 | 39.6% |
Reaction Steps
Sodium hydride (60 mg, 1.5 mmol) was added to a stirred suspension of 7-(2H-tetrazol-5-yl)-imidazo[1,2-a]pyridine (250 mg, 1.3 mmol) in dry DMF (4 ml) under a nitrogen atmosphere. After 1 h, Trifluoro-methanesulfonic acid 2,2,2-trifluoro-ethyl ester (1.16 g, 5 mmol) was added, followed by 18-crown-6 (260 mg, Immol). The reaction mixture was stirred at room temperature for 18 h then quenched with water and extracted with EtOAc (×2). The combined organic extracts were washed with brine (×1), dried (Na2SO4), filtered and the solvent removed in vacuo. Purification via silica column chromatography (0-2% 2M NH3MeOH/CH2Cl2) afforded the product (138 mg). MS: [M+H]+ 269.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895745B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-712f7928c90a44bbbb01a343c0ee2eef |
| Source note | uspto-grants-2014_11 |