HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonyl isocyanate → HCID 178498476, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonyl isocyanate | HCID 77703 | — |
| Reactant | HCID 178498498 | HCID 178498498 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178498476 | HCID 178498476 | 82.3% |
Reaction Steps
According to the procedure of Wright, Synthesis, 1984, 1058, methyl 4-hydroxy-2-quinolinecarboxylate (2.03 g, 0.01 m) and p-toluenesulfonyl isocyanate (1.97 g, 0.01 m) were mixed in reagent grade acetonitrile at RT. The heterogeneous mixture was heated at reflux until the evolution of COz had ceased (ca 2-3 hours). During this time a yellow solid formed. After cooling to RT, the yellow solid was collected by filtration, washed with acetonitrile, and dried to give methyl 4-(p-toluenesulfonylimino)-1,4-dihydroquinoline-2-carboxylate (2.93 g, 82%), melting point of 264°-265° C. (dec.), as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112821 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-f9de088f5f19412aa86e720f83208c9b |
| Source note | uspto-grants-1992_05 |