Sodium Hydroxide → 1-[(2R)-oxiranylmethyl]-4-methanesulfonylpiperazine

HRID 1675176Notes

Reaction equation

HRID 1675176 reaction equation
[OH-].[Na+].Cl[CH2:4][C@H:5]([OH:17])[CH2:6][N:7]1[CH2:12][CH2:11][N:10]([S:13]([CH3:16])(=[O:15])=[O:14])[CH2:9][CH2:8]1>C1COCC1.O>[O:17]1[CH2:4][C@H:5]1[CH2:6][N:7]1[CH2:12][CH2:11][N:10]([S:13]([CH3:16])(=[O:15])=[O:14])[CH2:9][CH2:8]1

Participants

4

Procedure

Sodium hydroxide (1.07 g, 26.7 mmol) was added to a vigorously stirred solution of 1-chloro-(R)-2-hydroxy-3-(4-methanesulfonylpiperazin-1-yl)propane, the product of the previous step (5.69 g, 22.2 mmol) in THF/water (150 mL/35 mL). The reaction mixture was stirred for 35 min, concentrated in vacuo to approximately 50 mL volume, diluted with chloroform (200 mL), and washed with 1M NaOH (2×70 mL) and brine (70 mL). The organic layer was dried (MgSO4), filtered and concentrated in vacuo to yield a white crystalline solid which was then recrystallised from hot EtOAc/hexane 1:1 (800 mL) to yield the title intermediate (2.62 g) as a white crystalline solid. (The filtrate could be further recrystallised to obtain additional product material.) ESMS (C8H16N2O3S): calcd. 221.10; found 221.3 (m/z): [M+H]+; 1H NMR (DMSO-d6): δ (ppm) 2.22 (dd, 1H), 2.45-2.60 (m, 5H), 2.69-2.75 (m, 2H), 2.87 (s, 3H), 3.02 (m, 1H), 3.11 (m, 4H).

Workup

  1. concentrationconcentrated in vacuo to approximately 50 mL volume
  2. additiondiluted with chloroform (200 mL)
  3. washwashed with 1M NaOH (2×70 mL) and brine (70 mL)
  4. dry with materialThe organic layer was dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto yield a white crystalline solid which
  8. customwas then recrystallised from hot EtOAc/hexane 1:1 (800 mL)

Sources & evidence

ORD record
ord-abc69c80408e4abe9aa8dac8aad850f7
Source dataset
uspto-grants-2011_08
Patent number
US08003664B2

Reaction notes

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