Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-[2-(4-Amino-furazan-3-yl)-imidazo[4,5-c]pyridin-1-yl]-phenol | HCID 57721189 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59681773 | HCID 59681773 | 2.4% |
Reaction Steps
To a solution containing 150 mg of the product from Example 38 (0.51 mmols) in 2.6 mL of dry DMF was added 25 mg of NaH (0.61 mmols, 60% suspension in oil). After stirring at ambient temperature for 5 min, 0.033 mL of chloroacetonitrile (0.51 mmols) was added to the reaction via syringe. The reaction was warmed to 60° C. for 16 h. After cooling to room temperature, 1 mL of water was carefully added to the reaction mixture. The mixture was diluted with 20 mL of EtOAc and washed with 2N NaOH (3×10 mL). The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The residue was dissolved in a minimum volume of DMSO and filtered through a 0.45 m acrodisc filter. The resulting solution was purified on the Gilson reverse-phase HPLC to afford the title product (4 mg, 2%). MS (ES+) m/e 334 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07348339B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-f4cd7fcc7762406d9e46b373a7498f59 |
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| Source note | uspto-grants-2008_03 |
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