Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | HCID 67915710 | HCID 67915710 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 67915830 | HCID 67915830 | — |
Reaction Steps
To a stirred solution of 5.01 parts of cis-4-amino-5-chloro-N-[1-(2-hydroxyethyl)-3-methoxy-4-piperidinyl]-2-methoxybenzamide in 112.5 parts of trichloromethane were added 1.33 parts of pyridine and 2 parts of thioyl chloride.. The whole was stirred and heated for 7 hours at 50° C. and subsequently stirred overnight at room temperature. The reaction mixture was washed with a sodium hydroxide solution and water. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated, yielding 9 parts of cis-4-amino-5-chloro-N-[1-(2-chloroethyl)-3-methoxy-4-piperidinyl]-2-methoxybenzamide monohydrate as a residue (interm. 15).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05130312 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-00b54a3a57584cfba686815ec09fa65f |
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| Source note | uspto-grants-1992_07 |
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