Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57450847 | HCID 57450847 | — |
| Reactant | HCID 86639782 | HCID 86639782 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Phthalamide | HCID 6956 | 194.4% |
Reaction Steps
4-Chloro-3-[(S)-1-methyl-2-methylthioethylimino]-3-H-isobenzofuran-1-one (0.2 g) and 6-(3,5-bis-trifluoromethyl-benzyl)-2-methyl-pyridin-3-ylamine (0.22 g) were dissolved in acetonitrile (10 ml), to which p-toluenesulfonic acid hydrate (0.01 g) was added, and stirred at 60° C. for 20 hours. After the reaction, the solvent was distilled off under reduced pressure and the resultant residue was purified by silica gel column chromatography to obtain N1-[6-3,5-bis-trifluoromethyl-benzyl)-2-methyl-pyridin-3-yl]-3-chloro-N2-(S)-1-methyl-2-methylhioethyl)phthalamide (0.21 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110689B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-119172765e964c5d8ea2b4d10d6daf3c |
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| Source note | uspto-grants-2012_02 |
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