Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chlorobenzenesulfonyl chloride | HCID 76187 | — |
| Reactant | HCID 18950754 | HCID 18950754 | — |
| Product | HCID 18950755 | HCID 18950755 | — |
Reaction Steps
To the solution of 4.98 g of 3-(4-methoxymethyloxyphenyl)-2-(3-pyridyl)propylamine and 100 ml of the solution of 2.22 g of triethylamine in methylene chloride was added 4.63 g of chlorobenzenesulfonyl chloride, and stirred at room temperature for four hours. The reaction mixture was poured into water, and the organic phase was separated which was then extracted with methylene chloride from aqueous phase. The combined organic phases were washed in saturated aqueous sodium chloride, and dried over magnesium sulfate, to distill off the solvent. The obtained residue was subjected to chromatography on a silica gel column, and from the fraction eluted with methanol-methylene chloride (5:95 v/v) was obtained 3.79 g of N-[3-(4-methoxymethyloxyphenyl)-2-(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-241df38cc1894f559ec9a878645efcbf |
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| Source note | uspto-grants-1994_12 |
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