Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-Methoxyazetidine | HCID 13401996 | — |
| Reactant | HCID 89922850 | HCID 89922850 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 89922670 | HCID 89922670 | 47.8% |
Reaction Steps
2-((2-chloro-5-cyano-4-(4-oxobutyl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (22 mg, 0.041 mmol) was taken up in THF (0.3 mL) and a solution of 3-methoxyazetidine (5.31 mg, 0.061 mmol) in MeOH (0.1 mL) was added, followed by a drop of AcOH and sodium cyanoborohydride (5.11 mg, 0.081 mmol). The reaction was stirred at room temperature for 1 h. The reaction was diluted with EtOAc and washed with water, then brine. The organic layer was dried over Na2SO4, filtered, and concentrated. The material was purified by flash column chromatography (0-7% MeOH/DCM; 24 g column). 2-((2-chloro-5-cyano-4-(4-(3-methoxyazetidin-1-yl)butyl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (12 mg) was obtained as a yellow glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273057B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-6bab8827a8f045be95d1aaa660a352db |
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| Source note | uspto-grants-2016_03 |
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