Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Cyclopropanemethanamine, N-propyl- | HCID 117787 | — |
| Reactant | 6-chloro-N-(2-methyl-4-(N-methylsulfamoyl)phenyl)pyrimidine-4-carboxamide | HCID 59446861 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 25183070 | HCID 25183070 | — |
Reaction Steps
A solution of 6-chloro-N-(2-methyl-4-(N-methylsulfamoyl)phenyl)pyrimidine-4-carboxamide (Intermediate 37, 80 mg; 0.235 mmol) and diisopropylamine (82 mL; 0.47 mmol) in ethanol (2.5 ml) was treated with N-(cyclopropylmethyl)propan-1-amine (0.7 ml; 0.29 mmol). The mixture was heated to 160° C. in a microwave for 1 hour and the solvent removed in vacuo. The residue purified by column chromatography (silica) eluting with petroleum ether containing increasing amounts of EtOAc to give the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150519B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-67499a5d251c4fc19803ca0420588905 |
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| Source note | uspto-grants-2015_10 |
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