Triethylamine → N-methoxy-4,N-dimethyl-3-sulfamoyl-benzamide

HRID 1810210Notes

Reaction equation

HRID 1810210 reaction equation
[CH3:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[S:11](=[O:14])(=[O:13])[NH2:12].Cl.[CH3:16][NH:17][O:18][CH3:19].C(N(CC)CC)C.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1>C(Cl)Cl>[CH3:19][O:18][N:17]([CH3:16])[C:6](=[O:7])[C:5]1[CH:9]=[CH:10][C:2]([CH3:1])=[C:3]([S:11](=[O:14])(=[O:13])[NH2:12])[CH:4]=1

Participants

6

Procedure

A mixture of 3.63 g of 4-methyl-3-sulfamoyl-benzoic acid, 1.92 g of N,O-dimethylhydroxylaminehydrochloride, and 5.02 mL of triethylamine in methylene chloride (120 mL) is treated with 8.32 g of benzotriazole-1-yl-oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate. The reaction mixture is stirred overnight at room temperature, washed sequentially with saturated aqueous sodium bicarbonate, water and a saturated sodium chloride solution, dried (magnesium sulfate) and concentrated in vacuo. The crude material is purified by silica gel chromatography (1:2 hexanes/ethyl acetate) to give N-methoxy-4,N-dimethyl-3-sulfamoyl-benzamide as a white powder. MS (m/z): 257 (M−1); Rf 0.25 (1:2 hexanes/ethyl acetate).

Workup

  1. washwashed sequentially with saturated aqueous sodium bicarbonate, water
  2. dry with materiala saturated sodium chloride solution, dried (magnesium sulfate)
  3. concentrationconcentrated in vacuo
  4. customThe crude material is purified by silica gel chromatography (1:2 hexanes/ethyl acetate)

Sources & evidence

ORD record
ord-38ee6a5d1e72449a87321e14ce95cb7a
Source dataset
uspto-grants-2013_01
Patent number
US08362063B2

Reaction notes

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