HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 14127915, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-5-(chloromethyl)pyridine | HCID 155479 | — |
| Reactant | HCID 178522584 | HCID 178522584 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14127915 | HCID 14127915 | 87% |
Reaction Steps
Dimethylformamide (2 mL) and tetrahydrofuran (18 mL) were added to 162 mg (0.82 mmol) of 2,2,2-trifluoro-N-(thiazolidin-2-ylidene)acetamide obtained by the above-described method, following which 198 mg of 2-chloro-5-chloromethylpyridine and 150 mg (1.09 mmol) of potassium carbonate were added, and the mixture was refluxed under heating for 20 hours. Following reaction completion, the reaction mixture was returned to room temperature, insoluble matter was filtered off, and the filtrate was concentrated under reduced pressure. The concentrate was purified on a TLC plate (two 0.5 mm plates, developed with 100% ethyl acetate), giving 230 mg of the target compound (yield, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328068B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-fc77e0e62ce4444bb2129e6060513c4d |
| Source note | uspto-grants-2016_05 |