HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923766Generated: October 27, 2026
Ammonia → 2-(2-ethylsulfanyl-phenyl)-6-heptafluoropropyl-3-methyl-3H-imidazo[4,5-b]pyridine
https://huagongshe.com/reaction/923766
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium perfluorobutanoate | HCID 23678859 | — |
| Reactant | 2-(2-ethylsulfanyl-phenyl)-6-iodo-3-methyl-3H-imidazo[4,5-b]pyridine | HCID 67981590 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-(2-ethylsulfanyl-phenyl)-6-heptafluoropropyl-3-methyl-3H-imidazo[4,5-b]pyridine | HCID 86708216 | 34.3% |
Reaction Steps
A mixture of 2-(2-ethylsulfanyl-phenyl)-6-iodo-3-methyl-3H-imidazo[4,5-b]pyridine (311 mg), copper iodide (1.5 g), sodium heptafluorobutyrate (1.8 g), NMP (5 ml), and xylene (25 ml) was stirred with heating at 150° C. for 12 hours. Into the reaction mixture cooled to room temperature, saturated aqueous sodium hydrogen carbonate solution and 28% aqueous ammonia were poured, and extracted with tart-butyl methyl ether. The combined organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 118 mg of 2-(2-ethylsulfanyl-phenyl)-6-heptafluoropropyl-3-methyl-3H-imidazo[4,5-b]pyridine (hereinafter referred to as Present Compound 128).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09278983B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-ae436b68d7e846088cab055ea95c7b40 |
|---|
| Source note | uspto-grants-2016_03 |
|---|