Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Amino-6-bromopyridine | HCID 300809 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Ethoxy-2-pyridinamine | HCID 586710 | — |
Reaction Steps
Introduced into a microwave tube are 500 mg (2.89 mmol) of 2-amino-6-bromopyridine, to which 2 ml of ethanol and 231 mg (5.78 mmol, 2 eq) of sodium hydroxide are added. The mixture is heated for 10 hours in a microwave oven at 170° C. The reaction medium is diluted with 50 ml of dichloromethane and then washed twice with 50 ml of water. The organic phase is concentrated to dryness and the residue is purified by chromatography over silica with, as eluent, heptane/ethyl acetate (1/1). The expected product is obtained in the form of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09050266B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-27634fa7300f49a98bb8830c44fe8199 |
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| Source note | uspto-grants-2015_06 |
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