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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686073Generated: October 27, 2026

3-(2,2-dipyridin-3-ylethyl)-N-methyl-N-pyridin-3-ylpyridin-2-amine → 2-{2-[Methyl(pyridin-3-yl)amino]pyridin-3-yl}-1,1-dipyridin-3-ylethanol

https://huagongshe.com/reaction/1686073

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2,2-dipyridin-3-ylethyl)-N-methyl-N-pyridin-3-ylpyridin-2-amineHCID 16662313—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDMSO t-BuOHHCID 86634320—
Product2-{2-[Methyl(pyridin-3-yl)amino]pyridin-3-yl}-1,1-dipyridin-3-ylethanolHCID 5786780073.3%

Reaction Steps

To a solution of 3-(2,2-dipyridin-3-ylethyl)-N-methyl-N-pyridin-3-ylpyridin-2-amine (34 mg) in 1.2 mL of DMSO:t-BuOH (80:20) was added potassium tert-butoxide (21 mg). The reaction was stirred under an oxygen balloon at room temperature for 2 h, then quenched by adding 2 drops of water. Purification by reverse phase HPLC gave 26 mg of 2-{2-[methyl(pyridin-3-yl)amino]pyridin-3-yl}-1,1-dipyridin-3-ylethanol as a white solid. 1H NMR (500 MHz, CDCl3): δ 8.54 (d, J=1.9 Hz, 2H), 8.47 (dd, J=4.6, 1.7 Hz, 2H), 8.35 (dd, J=4.6, 1.7 Hz, 1H), 8.21 (dd, J=4.6, 1.2 Hz, 1H), 8.05 (d, J=2.7 Hz, 1H), 7.59-7.57 (m, 2H), 7.24-7.15 (m, 4H), 7.08-7.05 (m, 1H), 6.99-6.95 (m, 1H), 4.57 (s, 1H), 3.55 (s, 2H), 3.21 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148535B2
Source datasetuspto-grants-2012_04
ORD IDord-1a0a0a198a25432c82e9570c2c1de03b
Source noteuspto-grants-2012_04