Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 12891577 | HCID 12891577 | — |
| Product | HCID 86737173 | HCID 86737173 | 16% |
Reaction Steps
A mixture of 3.7 parts of 1-(4-fluorophenylmethyl)-N-{1-[3-(4-methoxyphenylthio)propyl]-4-piperidinyl}-1H-benzimidazol-2-amine, 2.42 parts of hydrogen peroxide solution 30% and 20 parts of acetic acid is stirred and refluxed for 1 hour. The reaction mixture is cooled and poured onto ice-water. The whole is alkalized with sodium hydroxide solution 50% and the product is extracted with trichloromethane. The extract is washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is converted into the ethanedioate salt in methanol and 2-propanol. The salt is filtered off and dried, yielding 0.8 parts (16%) of 1-(4-fluorophenylmethyl)-N-{1-[3-(4-methoxyphenylsulfonyl)propyl]-4-piperidinyl}-1H-benzimidazol-2-amine ethanedioate (1:2); mp. 213.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04219559 |
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| Source dataset | uspto-grants-1980_08 |
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| ORD ID | ord-6c82d85dac7746578f227233fe662e64 |
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| Source note | uspto-grants-1980_08 |
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