HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 1,1-Diethyl-3-[13-(1,3-dithiolan-2-yl)-2,6-dimethyl-8alphaergolinyl]-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | 1,1-Ethanedithiol | HCID 33645 | — |
| Reactant | 1,1-Diethyl-3-(2,6-dimethyl-8alpha-ergolinyl)urea | HCID 14011011 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1-Diethyl-3-[13-(1,3-dithiolan-2-yl)-2,6-dimethyl-8alphaergolinyl]-urea | HCID 86748652 | — |
Reaction Steps
5.31 g of 1,1-diethyl-3-(2,6-dimethyl-8alpha-ergolinyl)-urea (15 mmol) is dissolved in 150 ml of chloroform and 50 ml of formic acid ethyl ester, 2.8 ml of ethanedithiol (33 mmol) and 60 ml of a 1 molar solution of titanium tetrachloride in dichloromethane (60 mmol) are added and stirred for 20 hours at room temperature. Then, it is mixed with 40 ml of methanol and 300 ml of water, made alkaline with 30 ml of 25% ammonia solution and shaken out with dichloromethane. The organic phases are dried with sodium sulfate, concentrated by evaporation and the residue is chromatographed on silica gel with dichloromethane/methanol. 4.14 g of substance, which crystallizes from ethyl acetate, is isolated, [α]D =-4° (0.5 % in chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05411966 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-fa9675f3aadc48238365a85657fbe7e7 |
| Source note | uspto-grants-1995_05 |