4-Methoxybenzenesulfonyl chloride → 4-[[4-Methoxybenzenesulfonyl]amino]-4-carbomethoxy-tetrahydrothiopyran

HRID 2209688Notes

Reaction equation

HRID 2209688 reaction equation
Cl.[NH2:2][C:3]1([C:9]([O:11][CH3:12])=[O:10])[CH2:8][CH2:7][S:6][CH2:5][CH2:4]1.C(N(CC)CC)C.[CH3:20][O:21][C:22]1[CH:27]=[CH:26][C:25]([S:28](Cl)(=[O:30])=[O:29])=[CH:24][CH:23]=1>C(Cl)Cl.O>[CH3:20][O:21][C:22]1[CH:23]=[CH:24][C:25]([S:28]([NH:2][C:3]2([C:9]([O:11][CH3:12])=[O:10])[CH2:4][CH2:5][S:6][CH2:7][CH2:8]2)(=[O:30])=[O:29])=[CH:26][CH:27]=1

Participants

6

Procedure

To a solution of 4-amino-4-carbomethoxy-tetrahydrothiopyran hydrochloride (3.1 g, 15.0 mmol) in methylene chloride (75 mL) containing triethylamine (3.5 g, 330.0 mmol) is added 4-methoxybenzenesulfonyl chloride (4.1 g, 20.0 mmol) at room temperature. The reaction mixture is stirred at room temperature for 18 hours. The mixture is diluted with water and the organic layer is removed. The aqueous layer is extracted with diethyl ether and the organic extracts are washed with brine, dried (MgSO4) and the solvent is evaporated. The product is purified by silica gel chromatography (50% ethylacetate/hexanes) to provide 4-[[4-methoxybenzenesulfonyl]amino]-4-carbomethoxy-tetrahydrothiopyran.

Workup

  1. customthe organic layer is removed
  2. extractionThe aqueous layer is extracted with diethyl ether
  3. washthe organic extracts are washed with brine
  4. dry with materialdried (MgSO4)
  5. customthe solvent is evaporated
  6. customThe product is purified by silica gel chromatography (50% ethylacetate/hexanes)

Sources & evidence

ORD record
ord-f4504b46dc484affbb57893e0ba4ac51
Source dataset
uspto-grants-1995_10
Patent number
US05455258

Reaction notes

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