Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 70455578 | HCID 70455578 | — |
| Product | HCID 12773702 | HCID 12773702 | — |
Reaction Steps
1,2,3,4-Tetrahydro-β-carboline-4-carboxylic acid hydrochloride (3 g, 0.012 mole) (TR-8025) prepared in Example 3 was mixed with 50 ml of methanol. It was cooled at 0° C. Then thionylchloride (2 ml, 0.028 mole) was added dropwise. The mixture was stirred at room temperature for 24 hours. The solvent was removed in vacuo. The residue was partitioned in ethyl acetate/6% K2CO3 solution. The organic phase was dried over MgSO4, filtered and treated with 4 NHCl in dioxane to pH=5. A white solid was collected. Yield: 2 g (62%) mp 246°-247° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04361566 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-e8e8b80ed5104e17b86ecb5ad3dbd9d3 |
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| Source note | uspto-grants-1982_11 |
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