HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 178521122, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178524710 | HCID 178524710 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 178521122 | HCID 178521122 | — |
Reaction Steps
3.8 ml of thionyl chloride were added to a suspension of 8.2 g of 4-hydroxy-quinoline-3-carboxylic acid in 160 ml of benzene and the mixture was refluxed for an hour and then cooled. The mixture was vacuum filtered and the precipiate was empasted with a little anhydrous benzene and was dried to obtain 9 g of 4-hydroxy-quinoline-3-carboxylic acid chloride melting at 260° C. The said product was then reacted with 4.35 g of 2-aminothiazole as in Example 1 to obtain 4.3 g of N-(2-thiazolyl)-4-hydroxy-quinoline-3-carboxamide melting at 349°-350° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04107310 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-09c62304b70d4e57afab9a53090f78e4 |
| Source note | uspto-grants-1978_08 |