Diethyl Ether → n-Hydroxy-1-[4-(4-chlorophenyl)-piperazine-1-sulfonyl]-piperidine-2-(rs)-carboxamide

HRID 1856874Notes

Reaction equation

HRID 1856874 reaction equation
FC(F)(F)C(O)=O.[O:8]([NH:16][C:17]([CH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][N:20]1[S:25]([N:28]1[CH2:33][CH2:32][N:31]([C:34]2[CH:39]=[CH:38][C:37]([Cl:40])=[CH:36][CH:35]=2)[CH2:30][CH2:29]1)(=[O:27])=[O:26])=[O:18])[Si](C(C)(C)C)(C)C.C(OCC)C>C(Cl)Cl>[OH:8][NH:16][C:17]([CH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][N:20]1[S:25]([N:28]1[CH2:33][CH2:32][N:31]([C:34]2[CH:35]=[CH:36][C:37]([Cl:40])=[CH:38][CH:39]=2)[CH2:30][CH2:29]1)(=[O:26])=[O:27])=[O:18]

Participants

5

Procedure

Trifluoroacetic acid (few drops) was added to a solution of N-tert-butyldimethylsiloxy-1-[4-(4-chlorophenyl)piperazine-1-sulfonyl]piperidine-2-(RS)-carboxamide (63 mg, 0.12 mmol), [prepared as described in Step 2 above], in methylene chloride (2 ml) and the reaction mixture was stirred at RT for 45 min. The organics were removed in vacuo and the residue was dissolved in methylene chloride (25 ml) and the washed with sat. sodium bicarbonate, brine, and dried over MgSO4. The solvent was removed in vacuo to give a foam which was redissolved in a minimum amount of methylene chloride. Diethyl ether was added and the resulting white precipitates were filtered to give N-hydroxy-1-[4-(4-chlorophenyl)-piperazine-1-sulfonyl]-piperidine-2-(RS)-carboxamide (67%).

Workup

  1. customThe organics were removed in vacuo
  2. dissolutionthe residue was dissolved in methylene chloride (25 ml)
  3. washthe washed with sat. sodium bicarbonate, brine
  4. dry with materialdried over MgSO4
  5. customThe solvent was removed in vacuo
  6. customto give a foam which
  7. customthe resulting white precipitates
  8. filtrationwere filtered

Sources & evidence

ORD record
ord-b8281121a1a2465781bfcf728bfb2e4c
Source dataset
uspto-grants-2000_11
Patent number
US06143744

Reaction notes

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