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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1668653생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1668653

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물(1H-indol-4-yl)methanamineHCID 280302—
반응물4-Chloro-2-(pyridin-2-yl)-6-(pyridin-3-yl)pyrimidineHCID 28309111—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물(1H-Indol-4-ylmethyl)-(6-pyridin-3-yl-2-pyridin-2-yl-pyrimidin-4-yl)-amineHCID 23653548—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07989458B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-b28b5156c4cc45c390324699be3e2f60
출처 메모uspto-grants-2011_08