HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (3RS)-2-[(Phenylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzenediazonium chloride | HCID 60992 | — |
| Reactant | 1,2,3,4-Tetrahydro-Beta-Carboline-3-Carboxylic Acid | HCID 98285 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | (3RS)-2-[(Phenylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid | HCID 13561960 | — |
Reaction Steps
(3RS)-1,2,3,4-Tetrahydro-β-carboline-3-carboxylic acid (3.24 g) is dissolved in dimethylsulfoxide (9 ml) and thereto is added 10N NaOH (33 ml) and further added carbon disulfide (0.91 ml) at room temperature. The mixture is stirred at room temperature for one hour, and to the mixture is added benzenediazonium chloride which is prepared from aniline (1.49 g), NaNO2 (1.15 g), conc. HCl (4.8 ml) and water (18.5 ml), and the mixture is stirred at 10° C. for one hour. The reaction mixture is treated in the same manner as described in Example 32. The product is crystallized from ethanol to give the title compound (676 mg) as pale yellow prisms, m.p. 167°-168° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04628057 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-50a04755e163489a8a424a87f0c1b357 |
| Source note | uspto-grants-1986_12 |