HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → HCID 44137768, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 44136066 | HCID 44136066 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 44137768 | HCID 44137768 | 35.6% |
Reaction Steps
To a suspension of 60 mg of crude 6-(2-bromoacetyl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in 10 mL of methanol are added 14 mg of thiourea. The reaction mixture is heated for 45 minutes at reflux and then concentrated to dryness under reduced pressure. The residue is chromatographed on a silica cartridge, eluting with a mixture of dichloromethane and methanol (gradient of from 100/0 to 90/10). The fractions containing the expected product are combined and evaporated to dryness under reduced pressure to give 20 mg of 6-(2-aminothiazol-4-yl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691990B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-d6c4caf7df704c5fb907fa0fe635becd |
| Source note | uspto-grants-2014_04 |