HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitro-6-phenylsulfanyl-imidazo[1,2-a]pyridine → HCID 53813641, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitro-6-phenylsulfanyl-imidazo[1,2-a]pyridine | HCID 54128243 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 53813641 | HCID 53813641 | — |
Reaction Steps
A solution of 0.542 gm. (0.002 mole) of 3-nitro-6-phenylthioimidazo [1,2-a] pyridine in 20 ml. of dioxane is reduced at 40 psi. under a hydrogen atmosphere with 0.500 g. of 5% palladium on carbon as catalyst. When the uptake of hydrogen is complete, the catalyst is removed by filtration. The filtrate is evaporated in vacuo to yield 3-amino-6-phenylthioimidazo [1,2-a] pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04237300 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-c4c0ffac28b4472aabeb70231a6e7b4a |
| Source note | uspto-grants-1980_12 |