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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668653Generated: October 25, 2026

Potassium Carbonate → (1H-Indol-4-ylmethyl)-(6-pyridin-3-yl-2-pyridin-2-yl-pyrimidin-4-yl)-amine

https://huagongshe.com/reaction/1668653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(1H-indol-4-yl)methanamineHCID 280302—
Reactant4-Chloro-2-(pyridin-2-yl)-6-(pyridin-3-yl)pyrimidineHCID 28309111—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(1H-Indol-4-ylmethyl)-(6-pyridin-3-yl-2-pyridin-2-yl-pyrimidin-4-yl)-amineHCID 23653548—

Reaction Steps

A solution of 4-chloro-6-pyridin-3-yl-2-pyridin-2-yl-pyrimidine (Intermediate A) (1 eq, 0.2 g), C-(1H-indol-4-yl)-methylamine (1.1 eq, 0.12 g) and K2CO3 (3 eq, 0.308 g) in NMP (6 ml) is heated using microwave radiation at 120° C. for 1 hour. After cooling to room temperature, the mixture is partitioned between EtOAc/water and the organic portion is separated, washed with brine, dried (MgSO4) and concentrated in vacuo. The crude residue is purified by mass directed preparative HPLC eluting with acetonitrile in water—0.1% TFA and the appropriate fractions are combined and concentrated in vacuo. The resulting residue is loaded onto a SCX-2 cartridge eluting with MeOH followed by 2M NH3 in MeOH. The methanolic ammonia fractions are concentrated in vacuo and dried under vacuum to afford the title compound [M+H]+=379.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989458B2
Source datasetuspto-grants-2011_08
ORD IDord-b28b5156c4cc45c390324699be3e2f60
Source noteuspto-grants-2011_08