Sodium hydride → HCID 22998392, compound

HRID 1738469Notes

Reaction equation

HRID 1738469 reaction equation
[NH2:1][C:2]1[O:6][N:5]=[C:4]([CH3:7])[C:3]=1[Br:8].[H-].[Na+].[O:11]1[CH:15]=[CH:14][CH:13]=[C:12]1[S:16](Cl)(=[O:18])=[O:17]>>[Br:8][C:3]1[C:4]([CH3:7])=[N:5][O:6][C:2]=1[NH:1][S:16]([C:12]1[O:11][CH:15]=[CH:14][CH:13]=1)(=[O:18])=[O:17]

Participants

4

Reactant 3

HCID 24758Sodium hydrideHCID 2795072Furan-2-sulfonyl ChlorideHCID 104875194-Bromo-3-methylisoxazol-5-amine

Product 1

HCID 22998392HCID 22998392, compoundYield 20%

Procedure

N-(4-bromo-3-methyl-5-isoxazolyl)furan-2-sulfonamide was prepared by the method of Example 1 with 5-amino-4-bromo-3-methylisoxazole (0.266 g, 1.5 mmol), NaH (60% oil dispersion) (0.15 g, 3.8 mmol) and furan-2-sulfonyl chloride (Example 36A) (0.30 mg, 1.8 mmol). Flash chromatography (50% EtOAc/hexane) and recrystallization from CHCl3 and hexane provided 90 mg (20% yield) of light yellow crystals (m.p. 117-119° C.).

Workup

  1. customFlash chromatography (50% EtOAc/hexane) and recrystallization from CHCl3 and hexane

Sources & evidence

ORD record
ord-94497dc6a9cf42d9974c9ddff7427de8
Source dataset
uspto-grants-1999_10
Patent number
US05962490

Reaction notes

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