Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 2-(Dimethylamino)ethanol | HCID 7902 | — |
| Reactant | 2-Chloropyridin-4-amine | HCID 84432 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 908117-05-5 | HCID 59244595 | — |
Reaction Steps
A mixture of 5.55 g of sodium and 26.9 mL of 2-dimethylaminoethanol in tetrahydrofuran (180 mL) is heated to reflux for 20 hours. The reaction mixture is cooled to room temperature, treated with 4 g of 4-amino-2-chloropyridine and heated to 140° C. for 20 min (microwave irradiation). The reaction mixture is treated with concentrated HCl to pH 8 at 0° C., saturated with sodium chloride and extracted with diethyl ether. The organics are dried (magnesium sulfate) and concentrated to 11.9 g of crude product which is purified by silica gel chromatography (90:10:1 ethyl acetate/methanol/ammonium hydroxide) to give 2-(2-dimethylamino-ethoxy)-pyridin-4-ylamine as tan crystals. MS (m/z): 182 (M+1); Rf 0.1 (90:10:1 ethyl acetate/methanol/ammonium hydroxide).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975439B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-9841aea82514498e975297f37a0cc5eb |
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| Source note | uspto-grants-2015_03 |
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