HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Bromo-8alpha-(3,3-diethylureido)-6-methyl-ergoline-13-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 3-(2-Bromo-6-methyl-8alpha-ergolinyl)-1,1-diethylurea | HCID 13059860 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-8alpha-(3,3-diethylureido)-6-methyl-ergoline-13-carbaldehyde | HCID 86748653 | — |
Reaction Steps
838 mg of 3-(2-bromo-6-methyl-8alpha-ergolinyl)-1,1-diethylurea (2 mmol) is dissolved in 100 ml of dichloromethane, 1.2 g of anhydrous aluminum chloride (9 mmol) and 1.8 ml of dichloromethyl methyl ether (20 mmol) are added and stirred for 15 minutes at room temperature. The reaction mixture is mixed with ice and, after 15 minutes, with a solution of 1.5 g of tartaric acid in 50 ml of water and made alkaline with 5 ml of conc. ammonia solution. It is extracted with dichloromethane, the organic phases are dried with sodium sulfate and the solvent is distilled off. The residue is chromatographed on silica gel with dichloromethane/methanol, 406 mg (45% of theory) is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05411966 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-8ac1f04fc7bf4b3182f969b016355951 |
| Source note | uspto-grants-1995_05 |