Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 67111881 | HCID 67111881 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 57397896 | HCID 57397896 | — |
Reaction Steps
To 2-(2-fluoro-4-(2-nitrovinyl)phenyl)-5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine (0.788 g, 1.89 mmol) was added THF (9.44 mL), methanol (9.44 mL), water (9.44 mL), and acetic acid (9.44 mL) before zinc (0.987 g, 15.1 mmol) was added. The reaction mixture was heated to 65° C. for 18 h. The reaction mixture was concentrated, neutralized with aq NaHCO3, and extracted with DCM. The organic layer was concentrated, filtered, washed with water, and dried in a vacuum oven to give the title compound after purification via preparatory LC. MS (ESI) m/z: Calculated: 389.1; Observed: 380.1 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07842685B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-86ceca96553749e3985faa39b7097cba |
|---|
| Source note | uspto-grants-2010_11 |
|---|