Sodium hydride → HCID 22004136, compound

HRID 1603855Notes

Reaction equation

HRID 1603855 reaction equation
O[C:2]1[CH:16]=[CH:15][C:5]2[N:6](C3C=CC=CC=3)[CH:7]=[N:8][C:4]=2[CH:3]=1.C1COCC1.[CH3:22][N:23]([CH:25]=[O:26])[CH3:24].[H-].[Na+].CN(C)C(Cl)=[S:32]>C1COCC1>[CH3:22][N:23]([CH3:24])[C:25](=[S:32])[O:26][C:7]1[NH:8][C:4]2[CH:3]=[CH:2][CH:16]=[CH:15][C:5]=2[N:6]=1

Participants

6

Reactant 4

HCID 24758Sodium hydrideHCID 27871Dimethylthiocarbamoyl chlorideHCID 6676621-Phenyl-1H-benzimidazol-5-olHCID 21974620tetrahydrofuran N,N-dimethylformamide

Product 1

HCID 22004136HCID 22004136, compoundYield 65%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
60 °C

Procedure

A solution of 5-hydroxy-1-phenylbenzimidazole (Example 14) (0.88 g, 4.10 mmol) in 1:1 THF/DMF (15 mL) was added dropwise under nitrogen to a stirred suspension of NaH (0.24 g of a 50% dispersion in oil, 5.00 mmol) in THF (10 mL). After 10 minutes a solution of dimethylthiocarbamyl chloride (0.57 g, 4.6 mmol) in THF (5 mL) was added and the solution was warmed at 60° C. for 1 hour. The cooled solution was partitioned between ether and 2N KOH and the organic portion was worked up and chromatographed on silica. Elution with EtOAc/petroleum ether (7:3) gave the O-benzimidazolyl dimethylthiocarbamate (0.76 g, 65%), mp (EtOAc/petroleum ether) 173-174.5° C.

Workup

  1. customThe cooled solution was partitioned between ether and 2N KOH
  2. customchromatographed on silica
  3. washElution with EtOAc/petroleum ether (7:3)

Sources & evidence

ORD record
ord-401b6d2c155e45e6a34cd1e5d7458eea
Source dataset
uspto-grants-1999_11
Patent number
US05990146

Reaction notes

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