Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | (6-Chloro-pyrido[3,2-d]pyrimidin-4-yl)-3-methyl-[1,2,4]thiadiazol-5-yl-amine | HCID 23160294 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Reactant | HCID 178527972 | HCID 178527972 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 178434789 | HCID 178434789 | 2.4% |
Reaction Steps
3-Mercapto-4H-[1,2,4]triazole (54 mg; 0.54 mmol) and 100 mg (0.36 mmol) of (6-chloro-pyrido[3,2-d]pyrimidin-4-yl)-3-methyl-[1,2,4]thiadiazol-5-yl-amine were added to a solution of 80 mg (0.72 mmol) of tert-butoxy potassium in 3 ml of N,N-dimethylacetamide and the mixture was stirred at 130° C. for 16 hours. Water was added to the reaction solution and the mixture was extracted with chloroform. The organic layer was dried and concentrated and the resulting residue was purified by a reversed phase preparative HPLC (0.1% TFA-containing water:acetonitrile=90:10→10:90) to give 3 mg (yield: 2%) of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687502B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-9e2d96fd6e9d44998cdf65a2f93b4a92 |
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| Source note | uspto-grants-2010_03 |
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