Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 18950734 | HCID 18950734 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18950693 | HCID 18950693 | — |
Reaction Steps
A 1.03 g portion of the thus obtained N-ethoxycarbonyl-N-[3-(4 -methoxymethyloxyphenyl)-3-(3-pyridyl)propyl]-4-chlorobenzenesulfonamide was dissolved in 25 ml of ethanol. After adding 1 ml of 6N hydrochloric acid, the solution was stirred at 60° C. for 1.5 hours. The resulting reaction mixture was concentrated under a reduced pressure, mixed with methylene chloride and then adjusted to alkalinity with saturated sodium hydrogencarbonate aqueous solution to separate organic layer. After extraction with chloroform, the extract was washed with saturated sodium chloride aqueous solution and dried using anhydrous magnesium sulfate. Thereafter, the solvent was removed by distillation under a reduced pressure to obtain 0.80 g of N-ethoxycarbonyl-N-[3-(4-hydroxyphenyl)-3-(3-pyridyl)propyl]-4-chlorobenzene sulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05374641 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-fb9880ab5a0a4a02aeb190cd50dee298 |
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| Source note | uspto-grants-1994_12 |
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