HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556319Generated: October 30, 2026
Potassium Carbonate → 3-(Benzo[d]thiazol-2-yl)-6-fluoroimidazo[1,2-a]pyridin-2-amine
https://huagongshe.com/reaction/556319
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Bromo-1,3-benzothiazole | HCID 612040 | — |
| Reactant | 2,2,2-Trifluoro-N-(6-fluoroimidazo[1,2-a]pyridin-2-yl)acetamide | HCID 25196649 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dioxan ethanol | HCID 22560076 | — |
| Product | 3-(Benzo[d]thiazol-2-yl)-6-fluoroimidazo[1,2-a]pyridin-2-amine | HCID 57607476 | — |
Reaction Steps
2,2,2-Trifluoro-N-(6-fluoro-imidazo[1,2-a]pyridin-2-yl)-acetamide (compound c, 6 g, 0.02 mol), 2-bromo-1,3-benzothiazole (6.8 g, 32 mmol), potassium carbonate (7000 mg, 0.05 mol), and triphenylphosphine (1000 mg, 0.005 mol) were diluted with 60 ml of a 2:1 solution of dioxane/ethanol and treated with palladium acetate (500 mg, 0.002 mol). The reaction was heated at 100° C. overnight. The reaction was cooled and resulting solid was filtered and washed with dichloromethane then dried to give 3-(benzo[d]thiazol-2-yl)-6-fluoroimidazo[1,2-a]pyridin-2-amine as a yellow solid. Rf 0.37, 70% ethyl acetate/hexanes; MS m/z 285 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058274B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-95b05aff0fa94b16a67aa981dc2f9f58 |
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| Source note | uspto-grants-2011_11 |
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