HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Formylmorpholine → N-(4-Morpholinylmethylene)-3-phenyl-1,2,4-thiadiazole-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Formylmorpholine | HCID 20417 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Phenyl-1,2,4-thiadiazole-5-sulfonamide | HCID 14183132 | — |
| Product | N-(4-Morpholinylmethylene)-3-phenyl-1,2,4-thiadiazole-5-sulfonamide | HCID 53678661 | — |
Reaction Steps
Thionyl chloride (4.5 ml) was added dropwise to 3.0 g of 3-phenyl-1,2,4-thiadiazole-5-sulfonamide in 15 ml of dry N-formylmorpholine at -5°. The resulting mixture was stirred at room temperature for 3 hours, poured into ice water and stirred for 15 minutes. The solids were collected, washed with water, dried, triturated with ether, washed with hexane and dried (in vacuo, P2O5). Recrystallization from benzene/hexane gave 1.1 g of solid, m.p. 185°-187°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985450 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-d033f2a879ef45e198c0af31bd2d14c0 |
| Source note | uspto-grants-1991_01 |