Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | K-604 | HCID 9892288 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86604311 | HCID 86604311 | 176.8% |
Reaction Steps
After heating and dissolving the free base (2.00 kg, 3.98 mol) of 2-[4-[2-(benzimidazol-2-ylthio)ethyl]piperazin-1-yl]-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]acetamide and pyridine hydrochloride (0.92 kg, 7.96 mol) in ethanol (12 L) at reflux temperature, water (20 L) was added dropwise to the reaction mixture at 75 to 87° C. The reaction mixture was allowed to cool down to room temperature, and was stirred for 1 hour. Precipitated crystals were collected by filtration. The crystals were washed with water and dried at 80° C. under reduced pressure to obtain 2-[4-[2-(benzimidazol-2-ylthio)ethyl]piperazin-1-yl]-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]acetamide monohydrochloride water adduct (1.96 kg, 89.0%; found to contain 2% of ethanol from 1H-NMR) as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518936B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-9307e189a6de4a7b92e29af9bffcf950 |
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| Source note | uspto-grants-2013_08 |
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