Water → HCID 86584941, compound

HRID 2308511Notes

Reaction equation

HRID 2308511 reaction equation
[CH3:1][O:2][C:3]1[C:8]2[N:9]=[C:10]([NH:12][C:13](=[O:20])[C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[S:11][C:7]=2[C:6]([N:21]2[CH2:26][CH2:25][S:24][CH2:23][CH2:22]2)=[CH:5][CH:4]=1.I([O-])(=O)(=O)=[O:28].[Na+].O.ClCCl>O1CCOCC1>[CH3:1][O:2][C:3]1[C:8]2[N:9]=[C:10]([NH:12][C:13](=[O:20])[C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[S:11][C:7]=2[C:6]([N:21]2[CH2:22][CH2:23][S:24](=[O:28])[CH2:25][CH2:26]2)=[CH:5][CH:4]=1

Participants

6

Procedure

To a solution of N-(4-methoxy-7-thiomorpholin-4-yl-benzothiazol-2-yl)-benzamide (80 mg, 0.21 mmol) in [1,4]dioxane (3 ml) was added sodium periodate (89 mg, 0.42 mmol) and the mixture stirred for 20 h at ambient temperature. To this mixture water (10 ml) and dichloromethane (10 ml) were added, the phases were separated and the aqueous layer extracted twice with dichloromethane. The combined organic extracts were dryed with Na2SO4 and the solvent evaporated. Recrystallization from hot THF afforded the title compound as white solid (21%), MS: m/e=402 (M+H+).

Workup

  1. customthe phases were separated
  2. extractionthe aqueous layer extracted twice with dichloromethane
  3. customthe solvent evaporated
  4. customRecrystallization from hot THF

Sources & evidence

ORD record
ord-8d3561ded664425b81e892e243e8d6f1
Source dataset
uspto-grants-2004_12
Patent number
US06835732B2

Reaction notes

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