HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bicarbonate Ion → 1,1-Diethyl-3-(2-iodo-6-methyl-8alpha-ergolinyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Terguride | HCID 443951 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1,1-Diethyl-3-(2-iodo-6-methyl-8alpha-ergolinyl)urea | HCID 13559030 | 76% |
Reaction Steps
A solution is prepared from 1 mmol of terguride in 20 ml of anhydrous dioxane, combined with about 1.5 ml of N-iodosuccinimide at room temperature and stirred for 30 minutes. The reaction mixture is then poured into a saturated bicarbonate solution, extracted with methylene chloride and the organic phase is dried with magnesium sulfate. After evaporation of the solvent, the residue is chromatographed on silica gel, thus obtaining in a 76% yield 1,1-diethyl-3-(2-iodo-6-methyl-8α-ergolinyl)urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04731367 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-020ebe24f10d4021b1ffeb30870c8fa2 |
| Source note | uspto-grants-1988_03 |