HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene glycol dioxane → 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)isonicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene glycol dioxane | HCID 22419261 | — |
| Reactant | 2-(3-(4-bromopyridin-2-yl)-1-(2-fluorobenzyl)-1H-1,2,4-triazol-5-yl)thiazole | HCID 69094285 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)isonicotinamide | HCID 69092904 | 11% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a stirring suspension of 2-(3-(4-bromopyridin-2-yl)-1-(2-fluorobenzyl)-1H-1,2,4-triazol-5-yl)thiazole (I-36, 1 equiv) in ethylene glycol-dioxane (approx. 4:1) in a sealed tube was added copper(I) cyanide (3 equiv). The resultant reaction mixture was heated at 100° C. for 24 hr and then cooled to room temperature, treated with brine and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated and purified using SiO2 chromatography (ethyl acetate/hexanes) to afford 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)isonicotinamide as a solid in 11% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09061030B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-462b5e32433448ea8a0ccb44da82d892 |
| Source note | uspto-grants-2015_06 |