Potassium Carbonate → HCID 15166240, compound

HRID 357546Notes

Reaction equation

HRID 357546 reaction equation
[SH:1][C:2]1[NH:6][C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[N:3]=1.Cl[CH2:12][C:13]1[C:18]([CH3:19])=[C:17]([O:20][CH2:21][CH2:22][N:23]2[C:27](=[O:28])[CH2:26][CH2:25][C:24]2=[O:29])[CH:16]=[CH:15][N:14]=1.C(=O)([O-])[O-].[K+].[K+]>C(C(C)=O)C>[CH3:19][C:18]1[C:13]([CH2:12][S:1][C:2]2[NH:6][C:5]3[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=3[N:3]=2)=[N:14][CH:15]=[CH:16][C:17]=1[O:20][CH2:21][CH2:22][N:23]1[C:27](=[O:28])[CH2:26][CH2:25][C:24]1=[O:29]

Participants

5

Procedure

A mixture comprising 0.03 g (0.18 mmol) of 2-mercapto-1H-benzimidazole, 0.06 g (0.21 mmol) of 2-chloromethyl-3-methyl-4-(2-succinimidoethoxy)pyridine, 0.03 g (0.21 mmol) of potassium carbonate and 10 ml of methyl ethyl ketone was heated under reflux in a nitrogen atmosphere for 3 hours, cooled and filtered. The filtrate was concentrated and dried in a vacuum, followed by the addition of water. The obtained mixture was extracted with 50 ml of chloroform thrice. The extract was dried over magnesium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography to obtain 0.08 g of 2-[{3-methyl-4-(2-succinimidoethoxy)pyridine-2-yl}methylthio]-1H-benzimidazole as a white crystal.

Workup

  1. temperatureunder reflux in a nitrogen atmosphere for 3 hours
  2. temperaturecooled
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated
  5. customdried in a vacuum
  6. additionfollowed by the addition of water
  7. extractionThe obtained mixture was extracted with 50 ml of chloroform thrice
  8. dry with materialThe extract was dried over magnesium sulfate
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated
  11. custompurified by silica gel column chromatography

Sources & evidence

ORD record
ord-d66ae517e24d476aa25708ae3db72e99
Source dataset
uspto-grants-1998_11
Patent number
US05840910

Reaction notes

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