Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 90031842 | HCID 90031842 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90031616 | HCID 90031616 | 97.2% |
Reaction Steps
0.238 g (0.949 mmol) of (3-(phenyl-ethynyl)imidazo[1,2-a]pyridin-2-yl) methanol were dissolved in 5 ml of dichloromethane with magnetic stirring and then 0.346 ml (4.75 mmol) of thionyl chloride were added. The mixture was stirred at r.t. for 2 h before being concentrated in vacuo. The residue was taken up into 20 ml of a mixture consisting of ethyl acetate and of a saturated NaHCO3 aqueous solution (1/1, v/v). After separation, the aqueous phase was extracted with 10 ml of ethyl acetate. The combined organic phases were washed with 10 ml of a saturated NaCl aqueous solution and then dried on Na2SO4 which was then removed by filtration. The obtained filtrate was concentrated in vacuo. 0.246 g (yield=96%) of 2-(chloromethyl)-3-(phenyl ethynyl)imidazo[1,2-a]pyridine were obtained as a brown solid. LC-MS: m/z=267 (MH+); UV purity at 254 nm=98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09381191B2 |
|---|
| Source dataset | uspto-grants-2016_07 |
|---|
| ORD ID | ord-c8f3980f72dd4e51afd3c79d54500e91 |
|---|
| Source note | uspto-grants-2016_07 |
|---|