HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 3,4-Dihydro-2H,6H-[1,3]thiazino[3,2-b]isoquinolin-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 12593121 | HCID 12593121 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 3,4-Dihydro-2H,6H-[1,3]thiazino[3,2-b]isoquinolin-6-one | HCID 171861 | — |
Reaction Steps
A mixture of 112 mg. of N-(3-mercaptopropyl)homophthalimide, 172 mg. of p-toluenesulfonic acid, and 4 ml. of o-dichlorobenzene was heated to 120° C. for 30 minutes. After cooling the reaction mixture, the solvent was distilled off from the reaction mixture under reduced pressure and the residue obtained was extracted with 50 ml. of benzene. The extract was washed with water, dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. By recrystallizing the residue thus obtained from isopropyl alcohol, 70 mg. of 6-oxo-3,4-dihydro-2H,6H-1,3-thiazino[3,2-b]isoquinoline was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163844 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-dbe1b8399d1641448a137de4e7874155 |
| Source note | uspto-grants-1979_08 |