Ammonia → HCID 70688908, compound

HRID 2247318Notes

Reaction equation

HRID 2247318 reaction equation
[C:1]([NH:4][C:5]1[S:6][C:7]([C:11]2[CH:16]=[CH:15][C:14]([S:17](Cl)(=[O:19])=[O:18])=[CH:13][CH:12]=2)=[C:8]([CH3:10])[N:9]=1)(=[O:3])[CH3:2].C(=O)([O-])[O-].[Na+].[Na+].[NH3:27].C(OCC)C>O1CCOCC1>[CH3:10][C:8]1[N:9]=[C:5]([NH:4][C:1](=[O:3])[CH3:2])[S:6][C:7]=1[C:11]1[CH:16]=[CH:15][C:14]([S:17](=[O:19])(=[O:18])[NH2:27])=[CH:13][CH:12]=1

Participants

6

Procedure

4-(2-Acetylamino-4-methyl-thiazol-5-yl)-benzenesulfonyl chloride (3a) (3.8 g, 11.5 mmol) is dissolved in dioxane (50 ml) with stirring. Sodium carbonate (2.45 g, 23 mmol) is added followed by a solution of ammonia in dioxane (50 ml, 0.75 M). After stirring for 2 hours at room temperature diethyl ether (120 ml) is added and the solid precipitate is removed by filtration. The solid is stirred in tetrahydrofuran (200 ml) and the mixture is then filtered through Celite™ filter material to remove inorganic material. Removal of the solvent affords N-[4-methyl-5-(4-sulfamoyl-phenyl)-thiazol-2-yl]-acetamide.

Workup

  1. additionis added
  2. customthe solid precipitate is removed by filtration
  3. stirringThe solid is stirred in tetrahydrofuran (200 ml)
  4. filtrationthe mixture is then filtered through Celite™
  5. filtrationfilter material
  6. customto remove inorganic material
  7. customRemoval of the solvent

Sources & evidence

ORD record
ord-0d12860da4664071a6e146ea1975f33a
Source dataset
uspto-grants-2010_03
Patent number
US07687637B2

Reaction notes

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