HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → 2-(Aminomethyl)-N-(2,4-dimethoxybenzyl)pyridin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 3-(2,4-Dimethoxybenzylamino)picolinonitrile | HCID 22293300 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Aminomethyl)-N-(2,4-dimethoxybenzyl)pyridin-3-amine | HCID 22293258 | 81% |
Reaction Steps
Lithium aluminum hydride (1.0 M in THF, 13.3 mL, 13.3 mmol) was added slowly to a solution of 3-[(2,4-dimethoxybenzyl)amino]pyridine-2-carbonitrile (3.25 g, 12.1 mmol) in tetrahydrofuran (40 mL) at 0° C. The reaction was warmed to room temperature and stirred for 4 h. The reaction was carefully quenched with a saturated aqueous solution of sodium sulfate, filtered with copious dichloromethane and concentrated to produce the title compound (2.68 g). MS 274.3 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745427B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-bf73fa5f9152432ca93d8dc7b871f2bd |
| Source note | uspto-grants-2010_06 |