HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 5-(4-Pyridylmethyloxy)-3-methylthio-1,2,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 4-Hydroxymethylpyridine | HCID 11472 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Chloro-3-(methylsulfanyl)-1,2,4-thiadiazole | HCID 570953 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-Pyridylmethyloxy)-3-methylthio-1,2,4-thiadiazole | HCID 12151389 | 54.4% |
Reaction Steps
Into 4 g of N,N-dimethylformamide was dissolved 218 mg of 4-pyridinemethanol, 96 mg of sodium hydride (60% in oil) was added thereto at room temperature. After stirring for 30 minutes, a solution of 334 mg of 5-chloro-3-methylthio-1,2,4-thiadiazole in 1 g of N,N-dimethylformamide was added dropwise into the mixture and the reaction mixture was stirred for 4 hours at room temperature. The reaction mixture was added to saturated sodium chloride aqueous solution, and extracted with t-butyl methyl ether. The organic layer was concentrated, and the residue obtained was subjected to silica gel column chromatography to give 260 mg of 5-(4-pyridylmethyloxy)-3-methylthio-1,2,4-thiadiazole (hereinafter, referred to as the present compound (34)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07273879B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-46688fcd0cd64a59b18c09ff254f94ed |
| Source note | uspto-grants-2007_09 |