HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040381Generated: November 1, 2026
Dimethylamine → 2-(2-(3-azidopropyl)-5-(2,5-difluorophenyl)-2-phenyl-1,3,4-thiadiazol-3(2H)-yl)-N,N-dimethylthiazole-4-carboxamide
https://huagongshe.com/reaction/2040381
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | ethyl 2-(2-(3-azidopropyl)-5-(2,5-difluorophenyl)-2-phenyl-1,3,4-thiadiazol-3(2H)-yl)thiazole-4-carboxylate | HCID 86608779 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-(3-azidopropyl)-5-(2,5-difluorophenyl)-2-phenyl-1,3,4-thiadiazol-3(2H)-yl)-N,N-dimethylthiazole-4-carboxamide | HCID 86649371 | — |
Reaction Steps
To a solution of dimethylamine (0.102 mL, 2.0 M, 0.2 mmol) in 1 mL of anhydrous THF was added trimethylaluminum (0.102 mL, 2.0 M, 0.2 mmol). The solution was stirred at room temperature for 15 minutes, then treated with a solution of ethyl 2-(2-(3-azidopropyl)-5-(2,5-difluorophenyl)-2-phenyl-1,3,4-thiadiazol-3(2H)-yl)thiazole-4-carboxylate (0.035 g, 0.07 mmol) in 0.5 mL of anhydrous THF. After stirring at room temperature for 16 hours the mixture was treated with 0.5N aqueous Rochelle's salt solution (10 mL), then partitioned between saturated NH4Cl (10 mL) and EtOAc (10 mL). The aqueous layer was extracted with EtOAc (2×10 mL) and the combined organic phases were washed with brine (10 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography (20-35% ethyl acetate/hexanes) to afford the desired product as a yellow gum, 0.026 g, 74%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08580828B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-6e6581f24bbd4d83bfd4ecd87f1fc81a |
|---|
| Source note | uspto-grants-2013_11 |
|---|