HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 67294556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67294688 | HCID 67294688 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67294556 | HCID 67294556 | — |
Reaction Steps
6-(4-(2-Aminoethoxy)-3-(trifluoromethyl)phenyl)-1-methyl-1H-[1,2,3]triazolo-[4,5-c]pyridine-4-carbonitrile (0.276 mmol, 0.1 g) and Hunig's base (0.828 mmol, 0.137 ml, 0.107 g) were stirred in THF (1 ml) at 0° C. acetyl chloride (0.552 mmol, 0.039 ml, 0.043 g) was added and the reaction was allowed to warm to room temperature and stirred for 1 hour. The resulting residue was taken up in DCM and washed with water. The organic was concentrated at reduced pressure. The resulting residue was purified by silica chromatography, eluting with DCM—3% MeOH/DCM to afford N-(2-(4-(4-cyano-1-methyl-1H-[1,2,3]triazolo[4,5-c]pyridin-6-yl)-2-(trifluoromethyl)phenoxy)ethyl)acetamide. (0.024 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115126B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-5f6dfed0b6004bfab411afbd6d97739e |
| Source note | uspto-grants-2015_08 |