Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 18349209 | HCID 18349209 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18348968 | HCID 18348968 | — |
Reaction Steps
To a solution of N-(3-amino-propyl)-3-chloro-N-isopropyl-5-[2-(pyridin-4-ylamino)-ethoxy]-benzamide trifluoroacetate (0.02 g) in dry acetonitrile (1 ml) was added a mixture of methanesulfonyl chloride (0.005 g) and triethylamine (0.017 ml) in acetonitrile (1 ml). The resultant mixture was stirred at room temperature for 15 h, and then concentrated under reduced pressure. The residue was stored in a mixture of dichloromethane (1 ml) and trifluoroacetic acid (2 ml) for 4 h, and then concentrated under reduced pressure. The residue was then subjected to preparative hplc and the title compound obtained as a colourless oil by concentration of the required fraction under reduced pressure and drying by repetitive addition of acetonitrile and concentration under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326386B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-cc2932d8e9814cbfa96bb26158c498bf |
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| Source note | uspto-grants-2001_12 |
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