HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Imidazo(1,2-a)pyrazine-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Imidazo(1,2-a)pyrazine | HCID 2771670 | — |
| Product | Imidazo(1,2-a)pyrazine-3-carbaldehyde | HCID 13634591 | — |
Reaction Steps
Imidazo[1,2-a]-pyrazine (0.30 g, 2.5 mmol) was dissolved in anhydrous DMF (10.0 mL) and added to a preformed solution of phosphorous oxychloride (0.26 mL, 2.8 mmol) in anhydrous DMF (10.0 mL). The solution was allowed to stir 72 h under nitrogen at RT. The solution was then poured into water (100 mL) and residual organics extracted with diethyl ether (3×30 mL). The remaining aqueous portion was concentrated to dryness under a nitrogen stream to yield the title compound (0.050 g). MS (ESI+) for m/z 148 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462600B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-827e7449345b4f2d936b529a177db2e8 |
| Source note | uspto-grants-2008_12 |