HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium iodide → 11beta-fluoro-3-hydroxy-7alpha-{5-[(2S)-2-(4-trifluoromethylphenylthiomethyl)-pyrrolidin-1-yl]-pentyl}-estra-1,3,5(10)-trien-17-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2S)-2-(4-trifluoromethylphenylthiomethyl)-pyrrolidine | HCID 57133071 | — |
| Reactant | HCID 68949346 | HCID 68949346 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 11beta-fluoro-3-hydroxy-7alpha-{5-[(2S)-2-(4-trifluoromethylphenylthiomethyl)-pyrrolidin-1-yl]-pentyl}-estra-1,3,5(10)-trien-17-one | HCID 57271395 | 57.2% |
Reaction Steps
A solution of 0.5 g of 7α-(5-chloropentyl)-11β-fluoro-3-hydroxy-estra-1,3,5(10)-trien-17-one in 4 ml of dimethylformamide is stirred with 0.55 g of (2S)-2-(4-trifluoromethylphenylthiomethyl)-pyrrolidine and 0.32 g of lithium iodide for 2 hours at a bath temperature of 100° C. Then, it is added to sodium bicarbonate solution, extracted three times with ethyl acetate, washed with common salt solution, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with dichloromethane/acetone. 0.45 g of 11β-fluoro-3-hydroxy-7α-{5-[(2S)-2-(4-trifluoromethylphenylthiomethyl)-pyrrolidin-1-yl]-pentyl}-estra-1,3,5(10)-trien-17-one with [α]D22 =+32.7° (c=0.51% in chloroform) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05986115 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-e28bdb318e5143f287e3798d59519df2 |
| Source note | uspto-grants-1999_11 |