Dehydroepiandrosterone → 1476-64-8

HRID 399729Notes

Reaction equation

HRID 399729 reaction equation
[CH3:1][C@@:2]12[C:10](=O)[CH2:9][CH2:8][C@H:7]1[C@@H:6]1[CH2:12][CH:13]=[C:14]3[CH2:19][C@@H:18]([OH:20])[CH2:17][CH2:16][C@:15]3([CH3:21])[C@H:5]1[CH2:4][CH2:3]2.C([O-])(=O)C.[Na+].Cl.C(OC(=O)[C@H](CS)N)C>C(O)C>[OH:20][C@H:18]1[CH2:17][CH2:16][C@@:15]2([CH3:21])[C:14](=[CH:13][CH2:12][C@@H:6]3[C@@H:5]2[CH2:4][CH2:3][C@@:2]2([CH3:1])[C@H:7]3[CH2:8][CH2:9][CH2:10]2)[CH2:19]1

Participants

5

Procedure

Following the procedure described by Djerassi (C. Djerassi, N. Crossley and M. A. Kielczewski, J. Org. Chem. 27, 1112, 1962), dehydroepiandrosterone (2.88 g, 10 mmol) is dissolved in anhydrous ethanol, sodium acetate is added followed by L-cysteine ethyl ester hydrochloride (18 g, 100 mmol) and the mixture is heated overnight under an argon atmosphere. The reaction mixture is then evaporated under vacuum. Methylene chloride is added to precipitate excess of L-cysteine ethyl ester hydrochloride. The solution is then filtered and the filtrate is washed twice with water, dried on magnesium sulfate, filtered and evaporated under vacuum. The residue is triturated with ethanol to give crystals.

Workup

  1. temperaturethe mixture is heated overnight under an argon atmosphere
  2. customThe reaction mixture is then evaporated under vacuum
  3. additionMethylene chloride is added to precipitate excess of L-cysteine ethyl ester hydrochloride
  4. filtrationThe solution is then filtered
  5. washthe filtrate is washed twice with water
  6. customdried on magnesium sulfate
  7. filtrationfiltered
  8. customevaporated under vacuum
  9. customThe residue is triturated with ethanol
  10. customto give crystals

Sources & evidence

ORD record
ord-96d2be2e162244e598187297bcd80b8a
Source dataset
uspto-grants-1998_10
Patent number
US05824671

Reaction notes

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