Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 70424265 | HCID 70424265 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131715239 | HCID 131715239 | 67.9% |
Reaction Steps
A mixture of 8.5 g of 6-methyl-8β-[N-(2-methoxycarbonyl-ethyl)aminomethyl]-ergoline (II: R1 =R2 =R3 =H, R4 =CH3, n=1, A=CH2 --CHR6, R6 =H, B=COOCH3 ; prepared as described in Example 1) and 2.86 g of potassium cyanate in 120 ml of water and 35 ml of 1N hydrochloric acid was heated at 60° C. for one hour. The solution was then neutralized with 1N sodium hydroxide and extracted with chloroform. The organic layer was evaporated off, and the residue was purified by column chromatography on silica gel, to give 6.5 g of the title compound. Rf in ethyl acetate:dimethylformamide:n-butanol:pyridine (4:3:3:1 by volume)=0.45; MS (F.D.): 384 (M+), 352 (M+ --CH3OH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04690929 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-30fb2be90a7d45fdab22a3540a10660b |
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| Source note | uspto-grants-1987_09 |
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