HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-(2-Bromo-13-iodo-6-methyl-8alpha-ergolinyl)-1,1-diethylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 3-(2-Bromo-6-methyl-8alpha-ergolinyl)-1,1-diethylurea | HCID 13059860 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 3-(2-Bromo-13-iodo-6-methyl-8alpha-ergolinyl)-1,1-diethylurea | HCID 67787849 | — |
Reaction Steps
42 mg of 3-(2-bromo-6-methyl-8alpha-ergolinyl)-1,1-diethylurea (0.1 mmol) is dissolved in 2 ml of trifluoroacetic acid and mixed with 22 mg of N-iodosuccinimide (0.1 mmol). After 15 minutes of stirring at room temperature, ice is added, it is made alkaline with ammonia, and shaken out with dichloromethane. The organic phases are dried and concentrated by evaporation, the residue is chromatographed. The pure substance crystallizes from dichloromethane, yield 9 mg (16% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05411966 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-4a800c25941c4f0aa35f3bce26941519 |
| Source note | uspto-grants-1995_05 |