HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → ethyl 2-(1-(4-cyanonaphthalen-1-yl)-1H-imidazol-2-ylthio)-2,2-difluoroacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Reactant | HCID 178510004 | HCID 178510004 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 2-(1-(4-cyanonaphthalen-1-yl)-1H-imidazol-2-ylthio)-2,2-difluoroacetate | HCID 59225900 | — |
Reaction Steps
Triethylamine (1.1 eq), followed by ethyl 2-bromo-2,2-difluoroacetate (1.05 eq) were added to a stirring slurry of 4-(2-mercapto-1H-imidazol-1-yl)-1-naphthonitrile (prepared as described herein, 1 eq) in dichloromethane and stirring continued for 3 h. The mixture was washed with aqueous HCl solution (0.2M), 50% saturated sodium chloride solution, dried over sodium sulfate, filtered, and concentrated. Hexanes were added and the mixture concentrated to provide ethyl 2-(1-(4-cyanonaphthalen-1-yl)-1H-imidazol-2-ylthio)-2,2-difluoroacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193234B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-2b0a786148ad47b296e6e9cc67051798 |
| Source note | uspto-grants-2012_06 |