Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251023Generated: October 26, 2026

3-Indol-1-yl-pyridine-2-carbonitrile → C-(3-Indol-1-yl-pyridin-2-yl)-methylamine

https://huagongshe.com/reaction/251023

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Indol-1-yl-pyridine-2-carbonitrileHCID 67271706—
CatalystNickelHCID 935—
SolventAmmoniaHCID 222—
ProductC-(3-Indol-1-yl-pyridin-2-yl)-methylamineHCID 6727329857.3%

Reaction Steps

A mixture of 3-indol-1-yl-pyridine-2-carbonitrile (164 mg, 0.75 mmol) in NH3 saturated MeOH (6 mL) was treated with Raney nickel (0.25 g), and placed under 40 psi H2 on a Parr shaker, for 4 h. The mixture was filtered through celite and the cake was washed with methanol. The eluant was concentrated under reduced pressure. Purification of the crude material by column chromatography on silica gel (CH2Cl2-MeOH, 96:4 then 9:1) provided 96 mg (57%) of C-(3-Indol-1-yl-pyridin-2-yl)-methylamine as a clear oil. 1H NMR (CDCl3) δ 1.65 (br s, 2H), 3.72 (s, 2H), 6.73 (d, 1H, J=3.3 Hz), 6.95-7.03 (m, 1H), 7.16-7.21 (m, 3H), 7.38 (dd, 1H, J=9, 6 Hz), 7.66-7.71 (m, 2H), 8.71 (d, 1H, J=4.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863293B2
Source datasetuspto-grants-2011_01
ORD IDord-286763f35eb14ef08860dc367c2320a9
Source noteuspto-grants-2011_01