HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → Isopropyl (3S)-2-[(4-chlorobenzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (3S)-2-[(4-Chlorobenzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid | HCID 13561935 | — |
| Product | Isopropyl (3S)-2-[(4-chlorobenzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylate | HCID 13562000 | — |
Reaction Steps
(3S)-2-[(4-Chlorobenzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (2.08 g) is suspended in isopropyl alcohol (30 ml) and thereto is added dropwise thionyl chloride (0.47 ml) at -20° C. The mixture is stirred at room temperature for 17 hours and then refluxed at 90° C. for 4 hours. After distilling off the solvent, the residue is dissolved in ethyl acetate. The solution is washed with water, dried and distilled to remove the solvent. The residue is recrystallized from ethyl acetate-n-hexane to give the title compound (477 mg), m.p. 178°-180° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04628057 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-47ce758d21f5410f80e4c9d12046a184 |
| Source note | uspto-grants-1986_12 |