Methyl 2-(2-sulfamoylphenyl)acetate → 2H-1,2-Benzothiazin-3(4H)-one

HRID 844922Notes

Reaction equation

HRID 844922 reaction equation
[S:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[CH2:11][C:12]([O:14]C)=O)(=O)(=O)[NH2:2]>[OH-].[Na+]>[S:1]1[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=2[CH2:11][C:12](=[O:14])[NH:2]1

Participants

3

Reactant 1

HCID 13064551Methyl 2-(2-sulfamoylphenyl)acetate

Product 1

HCID 218736702H-1,2-Benzothiazin-3(4H)-oneYield 96.4%

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent

Procedure

A solution of 18 g of 2-sulfamoylphenylacetic acid, methyl ester, in 125 g of 10% aqueous sodium hydroxide was stirred at room temperature for 4 hours. The mixture was filtered and the filtrate acidified by the addition of concentrated hydrochloric acid with ice-water cooling. The resulting precipitate was collected by filtration, washed with water, and dried to afford 12.5 g of 2H-1,2-benzothiazin-3(4H)-one, 1,1-dioxide as an off-white powder, m.p. 190°-195° C. NMR (CDCl3 /DMSO-d6): δ 11.3 (1H, br s, NH), 7.85 (1H, br d), 7.3-7.7 (3H, m) and 4.0 (2H, s).

Workup

  1. filtrationThe mixture was filtered
  2. additionthe filtrate acidified by the addition of concentrated hydrochloric acid with ice-water cooling
  3. filtrationThe resulting precipitate was collected by filtration
  4. washwashed with water
  5. customdried

Sources & evidence

ORD record
ord-888801a697174206bb6d2a5c06e9ac8e
Source dataset
uspto-grants-1988_07
Patent number
US04755211

Reaction notes

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