HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 2-(Furan-3-yl)imidazo[1,2-b][1,2,4]thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 54451730 | HCID 54451730 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Furan-3-yl)imidazo[1,2-b][1,2,4]thiadiazole | HCID 21514383 | — |
Reaction Steps
To 0.2 g. of 2-(3-furylthiocarbonylamino)-imidazole [(IV), R = 3-furyl] in 10 ml. of chloroform, at 20°-25°C, there is added dropwise 0.1 ml. of sulfuryl chloride in 2 ml. of chloroform. After 10 minutes the reaction mixture is concentrated at 10°-20°C. under vacuum to give a residue which is treated with methanol and filtered. The residue obtained following filtration is treated with dilute aqueous ammonia to give a precipitate which is filtered and dried to yield 2-(3-furyl)-1,2,4-thiadiazolo-[2,3-a]-imidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03979404 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-9fcb33bfe83c4566bc75027d7845c545 |
| Source note | uspto-grants-1976_09 |