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HRID 1668653作成日:2026年10月26日

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

https://huagongshe.com/reaction/1668653

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物(1H-indol-4-yl)methanamineHCID 280302—
反応物4-Chloro-2-(pyridin-2-yl)-6-(pyridin-3-yl)pyrimidineHCID 28309111—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物(1H-Indol-4-ylmethyl)-(6-pyridin-3-yl-2-pyridin-2-yl-pyrimidin-4-yl)-amineHCID 23653548—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07989458B2
出典データセットuspto-grants-2011_08
ORD IDord-b28b5156c4cc45c390324699be3e2f60
出典メモuspto-grants-2011_08