Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | HCID 58244031 | HCID 58244031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67024346 | HCID 67024346 | 124% |
Reaction Steps
5-chloro-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)benzoic acid (300 mg) was dissolved in DMF (9 ml), and WSC•monohydrochloride (200 mg), HOAt (140 mg) and cyclopropylamine (0.235 ml) were added thereto, followed by stiffing at room temperature for 2 hours. Water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with water and then saturated brine in this order, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting oily product was purified by silica gel column chromatography (chloroform:methanol=100:1). The resulting oily product was dissolved in ethyl acetate and 4M hydrogen chloride-ethyl acetate (1 ml) was added thereto, followed by concentrating under reduced pressure. The resulting solid was washed with ethyl acetate to obtain, as a white solid, 5-chloro-N-cyclopropyl-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)benzamide monohydrochloride (218 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377923B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d7492c1fc478473389e01371948d8dfd |
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| Source note | uspto-grants-2013_02 |
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