Dimethyl Sulfoxide → HCID 89924244, compound

HRID 2200359Notes

Reaction equation

HRID 2200359 reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[F:11][C:12]1[CH:17]=[CH:16][C:15]([N:18]2[CH2:23][CH2:22][N:21]([C:24]([CH3:28])([CH3:27])[CH2:25][OH:26])[CH2:20][CH2:19]2)=[CH:14][CH:13]=1.C(N(CC)CC)C>ClCCl.O>[F:11][C:12]1[CH:13]=[CH:14][C:15]([N:18]2[CH2:19][CH2:20][N:21]([C:24]([CH3:28])([CH3:27])[CH:25]=[O:26])[CH2:22][CH2:23]2)=[CH:16][CH:17]=1

Participants

7

Procedure

To a stirred solution of oxalyl chloride (0.7 mL, 8 mmol) in dichloromethane (30 mL) at −60° C. was added dropwise dimethylsulphoxide (1.1 mL, 15.5 mmol). The mixture was stirred for 2 min, and a solution of 2-(4-(4-fluorophenyl)piperazin-1-yl)-2-methylpropan-1-ol (1.5 g, 4.9 mmol) in dichloromethane (10 mL) was then added. The reaction mixture was stirred for 15 min, triethylamine (5 mL, 25.5 mmol) was added. The reaction mixture was stirred for 5 min and then allowed to warm to room temperature. Water (100 mL) was then added and the aqueous layer was extracted with additional dichloromethane (100 mL). The organic layers were combined, washed sequentially with brine (200 mL), dried over sodium sulphate and evaporated till dryness. The crude product was purified by column chromatography over silica gel (100-200 mesh) using 10% ethylacetate in hexane to obtain the title compound (1.2 g, 83.0%).

Workup

  1. stirringThe reaction mixture was stirred for 15 min
  2. stirringThe reaction mixture was stirred for 5 min
  3. extractionthe aqueous layer was extracted with additional dichloromethane (100 mL)
  4. washwashed sequentially with brine (200 mL)
  5. dry with materialdried over sodium sulphate
  6. customevaporated till dryness
  7. customThe crude product was purified by column chromatography over silica gel (100-200 mesh)

Sources & evidence

ORD record
ord-eb34d7b3cd554accbbb6aba9f7feb516
Source dataset
uspto-grants-2016_06
Patent number
US09359367B2

Reaction notes

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