Water → HCID 9844021, compound

HRID 1647628Notes

Reaction equation

HRID 1647628 reaction equation
C1(=O)[N:5]([CH2:6][CH2:7][O:8][C@H:9]2[CH2:26][CH2:25][C@@:24]3([CH3:27])[C@H:11]([CH2:12][CH2:13][C@@H:14]4[C@@H:23]3[CH2:22][CH2:21][C@@:19]3([CH3:20])[C@:15]4([OH:33])[CH2:16][CH2:17][C@@H:18]3[C:28]3[CH:32]=[CH:31][O:30][CH:29]=3)[CH2:10]2)C(=O)C2=CC=CC=C12.O.NN.O>C(O)C>[NH2:5][CH2:6][CH2:7][O:8][C@H:9]1[CH2:26][CH2:25][C@@:24]2([CH3:27])[C@H:11]([CH2:12][CH2:13][C@@H:14]3[C@@H:23]2[CH2:22][CH2:21][C@@:19]2([CH3:20])[C@:15]3([OH:33])[CH2:16][CH2:17][C@@H:18]2[C:28]2[CH:32]=[CH:31][O:30][CH:29]=2)[CH2:10]1

Participants

5

Procedure

To a solution of 0.50 g of 3β-(2-phthalimidoethoxy)-17β-(3-furyl)-5β-androstan-14β-ol in 50 ml of ethanol (96%) 0.19 g of hydrazine hydrate were added at room temperature. The mixture was kept at reflux for 4 hrs, then 10 ml of water were added and the ethanol distilled under reduced pressure. The residue was extracted with methylene chloride, the organic solution was washed with water, dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The crude residue was purified by flash-chromatography (SiO2) using methylene chloride/methanol 90/10 as eluant to give 0.35 g of the title compound (I-aa) as a white solid.

Workup

  1. temperatureat reflux for 4 hrs
  2. distillationthe ethanol distilled under reduced pressure
  3. extractionThe residue was extracted with methylene chloride
  4. washthe organic solution was washed with water
  5. dry with materialdried over anhydrous sodium sulfate
  6. customevaporated to dryness under reduced pressure
  7. customThe crude residue was purified by flash-chromatography (SiO2)

Sources & evidence

ORD record
ord-05a16deb060146028fd3deb71a795bdf
Source dataset
uspto-grants-1995_07
Patent number
US05432169

Reaction notes

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