HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 5-(Aminomethyl)pyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-Amino-5-cyanopyridine | HCID 818260 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 5-(Aminomethyl)pyridin-2-amine | HCID 15766771 | 83.1% |
Reaction Steps
To a solution of 6-aminonicotinonitrile 117-A (5.0 g, 42 mmol) was added a solution of 1 M BH3-THF (294 mL, 294 mmol) at 0° C. (prepared as in J.Org. Chem., Vol. 38, No. 5, 1973). The reaction was stirred at room temperature for 1 hour. The reaction mixture was then slowly pored into ice water. 100 mL 4N HCl was added and stirred for 20 min. The solution was basified with NH4OH to pH of about 11, and then concentrated. THF (300mL×2) was added to the mixture followed by addition of solid KOH (excess). The suspension was stirred. The THF layer was collected by filtration and concentrated to give 5-(aminomethyl)pyridin-2-amine 117-B (4.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07381824B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-dc84e24aea9d480893515ad0ec3b381a |
| Source note | uspto-grants-2008_06 |