1,3-Benzodioxole-5-carboxylic acid → HCID 10839533, compound

HRID 234412Notes

Reaction equation

HRID 234412 reaction equation
C(N1C=CN=C1)(N1C=CN=C1)=O.[C:13]([OH:24])(=O)[C:14]1[CH:22]=[CH:21][C:20]2[O:19][CH2:18][O:17][C:16]=2[CH:15]=1.[Br:25][C:26]1[C:27]([CH3:43])=[N:28][O:29][C:30]=1[NH:31][S:32]([C:35]1[CH:39]=[CH:38][S:37][C:36]=1[C:40]([NH2:42])=[O:41])(=[O:34])=[O:33].[H-].[Na+]>C1COCC1.O>[Br:25][C:26]1[C:27]([CH3:43])=[N:28][O:29][C:30]=1[NH:31][S:32]([C:35]1[CH:39]=[CH:38][S:37][C:36]=1[C:40]([NH:42][C:13](=[O:24])[C:14]1[CH:22]=[CH:21][C:20]2[O:19][CH2:18][O:17][C:16]=2[CH:15]=1)=[O:41])(=[O:34])=[O:33]

Participants

7

Reactant 4

HCID 71961,3-Benzodioxole-5-carboxylic acidHCID 24758Sodium hydrideHCID 682631,1'-CarbonyldiimidazoleHCID 10546830HCID 10546830, compound

Product 1

HCID 10839533HCID 10839533, compoundYield 3.6%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Procedure

Carbonyldiimidazole (21 3 mg. 1.31 mmol) was added to a solution of piperonylic acid (181.5 mg., 1.09 mmol) in dry THF (10 ml). The resulting mixture was stirred for 15 minutes. N-(4-bromo-3-methyl-5-isoxazolyl)-2-aminocarbonylthiophene-3-sulfonamide (Example 89) (400 mg, 1.09 mmol) and NaH (175 mg, 60% in mineral oil, 4.37 mmol) were added sequentially. The mixture was stirred at room temperature for 8 hours. Water was added to destroy the excess NaH. The solvent was then evaporated and the residue was partitioned between 1N HCl and EtOAc. The organic layer was dried (MgSO4), the solid filtered and the filtrate concentrated. The residue was recrystalized from EtOAc to give N-(4-bromo-3-methyl-5-isoxazolyl)-2-{[(3,4-methylenedioxy)benzoyl]aminocarbonyl}thiophene-3-sulfonamide (20 mg, 3.6% yield) as a yellowish powder (m.p. 90°-93° C.).

Workup

  1. stirringThe mixture was stirred at room temperature for 8 hours
  2. customto destroy the excess NaH
  3. customThe solvent was then evaporated
  4. customthe residue was partitioned between 1N HCl and EtOAc
  5. dry with materialThe organic layer was dried (MgSO4)
  6. filtrationthe solid filtered
  7. concentrationthe filtrate concentrated
  8. customThe residue was recrystalized from EtOAc

Sources & evidence

ORD record
ord-94aefd94dc944e91a47d59ba13ee77be
Source dataset
uspto-grants-1997_01
Patent number
US05594021

Reaction notes

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