5-Amino-3-methylisoxazole → N-(3-methyl-5-isoxazolyl)-5-bromothiophene-2-sulfonamide

HRID 2270724Notes

Reaction equation

HRID 2270724 reaction equation
[Br:1][C:2]1[S:6][C:5]([S:7](Cl)(=[O:9])=[O:8])=[CH:4][CH:3]=1.[NH2:11][C:12]1[O:16][N:15]=[C:14]([CH3:17])[CH:13]=1>>[CH3:17][C:14]1[CH:13]=[C:12]([NH:11][S:7]([C:5]2[S:6][C:2]([Br:1])=[CH:3][CH:4]=2)(=[O:9])=[O:8])[O:16][N:15]=1

Participants

3

Reactant 2

HCID 845905-Amino-3-methylisoxazoleHCID 27339245-Bromothiophene-2-sulfonyl chloride

Product 1

HCID 22998516N-(3-methyl-5-isoxazolyl)-5-bromothiophene-2-sulfonamide

Procedure

N-(3-methyl-5-isoxazolyl)-5-bromothiophene-2-sulfonamide was prepared in the same manner as described in Example 14 from 5-bromothiophene-2-sulfonyl chloride and 5-amino-3-methyl isoxazole. Purification was achieved by extraction of the crude sulfonamide into aqueous 2N NaOH, washing of the aqueous layer with ethyl acetate and acidification, using concentrated HCl, to pH˜2. Re-extraction into ethyl acetate was followed by washing of the organic material with water, brine and drying over magnesium sulfate. After evaporation of solvents, a brownish solid remained which was sufficiently pure to use in the next step.

Workup

  1. customPurification
  2. extractionwas achieved by extraction of the crude sulfonamide into aqueous 2N NaOH
  3. washwashing of the aqueous layer with ethyl acetate and acidification
  4. washby washing of the organic material with water, brine
  5. dry with materialdrying over magnesium sulfate
  6. customAfter evaporation of solvents

Sources & evidence

ORD record
ord-01ff8d1b316a4b828e6d011a911c4a90
Source dataset
uspto-grants-2001_12
Patent number
US06331637B1

Reaction notes

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