Hydrochloric Acid → HCID 86754947, compound

HRID 366408Notes

Reaction equation

HRID 366408 reaction equation
C([O:4][C@H:5]1[CH2:10][CH2:9][C@H:8]2[C@H:11]3[C@H:20]([CH2:21][CH2:22][C@:6]12[CH3:7])[C:19]1[CH:18]=[CH:17][C:16]([O:23]C(=O)C2C=CC=CC=2)=[CH:15][C:14]=1[CH2:13][C@H:12]3[CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][N:40]1[C:44]([CH3:46])([CH3:45])[C:43]2[CH:47]=[CH:48][CH:49]=[C:50]([N+:51]([O-:53])=[O:52])[C:42]=2[Se:41]1)(=O)C.[OH-].[Na+].Cl>C1COCC1.CO>[OH:23][C:16]1[CH:17]=[CH:18][C:19]2[C@@H:20]3[C@H:11]([C@H:8]4[C@@:6]([CH2:22][CH2:21]3)([CH3:7])[C@@H:5]([OH:4])[CH2:10][CH2:9]4)[C@H:12]([CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][N:40]3[C:44]([CH3:45])([CH3:46])[C:43]4[CH:47]=[CH:48][CH:49]=[C:50]([N+:51]([O-:53])=[O:52])[C:42]=4[Se:41]3)[CH2:13][C:14]=2[CH:15]=1

Participants

6

Procedure

N-{8-[17β-acetoxy-3-benzoyloxyestra-1,3,5(10)-trien-7α-yl]octyl}-3,3-dimethyl-7-nitrobenzisoselenazoline (115 mg, 0.15 mmol) is dissolved in 2 ml of THF and 1 ml of methanol. To the obtained mixture is then added an aqueous solution of NaOH (1 ml, 1N, 1.0 mmol). The reaction medium is stirred at room temperature for 22 hours, then neutralized with an aqueous solution of HCl (1N). The mixture is extracted with ethyl acetate. The combined organic phases are washed with a saturated aqueous solution of NaCl, dried over MgSO4 and evaporated. The residue is purified by silica gel column chromatography (eluent:EtOAc:cyclohexane, 1:3) to provide the expected product (95 mg, 94%) as a deep red solid.

Workup

  1. extractionThe mixture is extracted with ethyl acetate
  2. washThe combined organic phases are washed with a saturated aqueous solution of NaCl
  3. dry with materialdried over MgSO4
  4. customevaporated
  5. customThe residue is purified by silica gel column chromatography (eluent:EtOAc:cyclohexane, 1:3)

Sources & evidence

ORD record
ord-8f87d6e7a43849ef97b853a26f8abfe6
Source dataset
uspto-grants-2000_10
Patent number
US06130212

Reaction notes

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