Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | O,O-Diethyl dithiophosphate | HCID 9274 | — |
| Reactant | HCID 28325782 | HCID 28325782 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 82530452 | HCID 82530452 | 86.9% |
Reaction Steps
To a suspension of 6-bromo-2-methylimidazo[1,2-a]pyridine-3-carbonitrile (6.2 g, 26.4 mmol) obtained above in MeOH (88 mL), were added 4N solution of hydrogen chloride in EtOAc (22 mL, 88.0 mmol) and O,O-diethyl hydrogen dithiophosphate (25 mL, 158 mol), and the mixture was stirred at 60° C. for 3 h. The mixture was allowed to cool to rt, and diluted with diisopropyl ether (100 mL). The resulting precipitate was collected by filtration and washed with diethyl ether to give the title compound (6.2 g, 77%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139589B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-551bb939adc742c6a37b0bc6d084d28e |
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| Source note | uspto-grants-2015_09 |
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