Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloropropionyl chloride | HCID 111019 | — |
| Reactant | 2-Amino-5-cyanopyridine | HCID 818260 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 44574294 | HCID 44574294 | — |
Reaction Steps
To a suspension of 2-amino-5-cyanopyridine (0.500 g, 4.2 mmol) in dry dichloromethane (20 mL) was added triethylamine (0.830 g, 6.3 mmol) and the mixture was stirred at 0° C. To the reaction mixture, 2-chloropropionyl chloride (0.800 g, 6.3 mmol) was added dropwise, and the reaction mixture was stirred at 0° C. for an hour and then at room temperature for 48 hours. The reaction mixture was diluted with dichloromethane (100 mL) and was washed with water (150 mL). The reaction mixture was dried over anhydrous sodium sulfate and concentrated to obtain the crude product, which was purified by column chromatography (silica gel, 15-20% ethyl acetate in petroleum ether as an eluent) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314103B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-2cc7b6b7adcc41ceaa2c0a1f37fa61f1 |
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| Source note | uspto-grants-2012_11 |
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