Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 19737951 | HCID 19737951 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 17875048 | HCID 17875048 | 53.3% |
Reaction Steps
The product from Step C (1 g, 3 mmol) was dissolved in tetrahydrofuran (50 mL) containing triethylamine (1.7 mL, 12.0 mmol) and the solution was cooled to -16° C. Tosyl chloride (1.1 g, 6.0 mmol) was added and the mixture stirred for 18 h at room temperature after which time it was cooled to 0° C. and ethylamine (10 mL) was added. After heating at reflux for 1 h the solvent was evaporated and the residue dissolved in ethyl acetate (50 mL) and washed with 1N HCL (3×20 mL). The combined aqueous washes were basified (sodium bicarbonate) and extracted with ethyl acetate. The combined extracts were washed with saturated sodium bicarbonate solution (3×15 mL) and brine (3×15 mL), dried (MgSO4) and evaporated to give the desired free base (620 mg) as a syrup. This material was dissolved in ethanol (5 mL) and IN ethanolic HCL (5 mL) was added. This solution was then concentrated to dryness to give the desired product as a light yellow solid (400 mg): mp 243°-245° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05240923 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-0e16061764734d6ca7589782b0d8b483 |
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| Source note | uspto-grants-1993_08 |
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