HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647638Generated: October 25, 2026
Water → 3beta-(2-(N-(2-(1-Pyrrolidinyl)ethyl)methylamino)ethylthio)-17beta-(3-furyl)-5beta-androstan-14beta-ol
https://huagongshe.com/reaction/1647638
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl(2-(pyrrolidin-1-yl)ethyl)amine | HCID 295976 | — |
| Reactant | 3beta-(2-Tosyioxyethylthio)-17beta-(3-furyl)-5beta-androstan-14beta-ol | HCID 86748785 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3beta-(2-(N-(2-(1-Pyrrolidinyl)ethyl)methylamino)ethylthio)-17beta-(3-furyl)-5beta-androstan-14beta-ol | HCID 70046027 | 60.7% |
Reaction Steps
To a solution of 0.34 g of N-(2-(1-pyrrolidinyl)ethyl) methylamine in 5 ml of dimethylformamide, 0.045 g of NaH (60% dispersion in mineral oil) were added under nitrogen and the mixture was stirred at room temperature for half an hr; a solution of 0.50 g of 3β-(2-tosyloxyethylthio)-17β-(3-furyl)-5β-androstan-14β-ol, prepared as described in Ex. 51, in 2 ml of dimethylformamide was added, the mixture was stirred for another 4 hrs and then 7 ml of water were poured in. The residue was extracted with ethyl acetate, the organic solution was washed with water to neutral pH, dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The crude product was purified by flash-chromatography (SiO2) using methylene chloride/methanol 95/5 as eluant to give 0.28 g of the title compound (I-ca)as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05432169 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-509622baa2334647a31641295bd5bfbd |
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| Source note | uspto-grants-1995_07 |
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