Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 10286610 | HCID 10286610 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178508137 | HCID 178508137 | 10% |
Reaction Steps
To a one dram vial was added 20 mg (0.0604 mmol) of 3-(benzenesulfonyl)-2-methylsulfanyl-pyrido[1,2-a]pyrimidin-4-ylideneamine and 1.1 equivalents of ethanolamine in 750 ml of DMF. The vial was fitted with a TEFLON® lined cap and heated to 55° C. over night. The resulting product was then purified on a reverse phase preparative HPLC (XTerra™ MS C18 5.0 mM, MeOH/H2O as the eluent) to give 23 mg of the title compound as a brown solid; 10% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875771B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-8663fc3d71e347adad3df0f4f7c549ec |
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| Source note | uspto-grants-2005_04 |
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