Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | 2-(2-Aminophenethyl)-1-methylpiperidine | HCID 11085282 | — |
| Reactant | HCID 85370880 | HCID 85370880 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Potassium Acetate | HCID 517044 | — |
| Product | Encainide hydrochloride | HCID 48040 | — |
Reaction Steps
A process for preparing 4-methoxy-2'-[2-(1-methyl-2-piperidyl) ethyl]benzanilide (I) as the hydrochloride salt ##STR4## which comprises (a) combining α-picoline and dimethylsulfate to form the picolinium methyl sulfate salt (V) ##STR5## which is then reacted with o-nitrobenzaldehyde to produce 1-(2-nitrophenyl)-2-[2-1-methyl) pyridinium methyl sulfate]-ethanol (IV) ##STR6## (b) dehydrating (IV) by heating in a mixture of acetic acid, acetic anhydride and potassium acetate to yield 2-(2-nitrostyrenyl)-[2-(1-methyl) pyridinium methyl sulfate ] (III); ##STR7## (c) hydrogenating (III) using a platinum catalyst to generate 2-(2-aminophenethyl)-1-methylpiperidine (II); and ##STR8## (d) reacting (II) with anisoyl chloride in an organic solvent selected from the group consisting of acetone, acetonitrile, and a C2-5 alkanol, to obtain encainide hydrochloride directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04675409 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-9f54906643bf4aa6ba48a5c9575ef91f |
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| Source note | uspto-grants-1987_06 |
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