Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 23520037 | HCID 23520037 | — |
| Reactant | HCID 66871793 | HCID 66871793 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66871873 | HCID 66871873 | — |
Reaction Steps
To a mixture of 2-oxo-3-hydroxy lysergic acid Nethyl N-(2-carbethoxy)ethyl amide 7 (63.6 mg, 0.15 mmol) in 5 ml of tetrahydrofuran (THF) and 5 ml of water was added solid potassium hydroxide (12.5 mg, 0.22 mmol). The reaction was stirred at room temperature for 3 hours (h) until the reaction was complete by TLC analysis. The reaction solution was neutralised to pH 7 using 1N HCl and concentrated to dryness under reduced pressure. The residue was dissolved in a 10% methanol in chloroform mixture and the inorganic salts were removed by filtration. Evaporation of the solvents yielded 2-oxo-3-hydroxy lysergic acid N-ethyl N-(2-carboxy)ethyl amide (Hapten A) (45 mg, 76%) as an amorphous brown solid (Rf 0.52 on silica using 20% methanol in chloroform as eluent). υmax/cm−1 3297, 2963, 1723, 1557, 1099, 1026, 802 (FT-IR)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115718B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-7ab750337c684da7912f2ca767c4b27f |
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| Source note | uspto-grants-2006_10 |
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