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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31741생성일: 2026년 10월 24일

Diethyl Ether → 4-(2-{[2-(2-Pyridylamino)ethyl]amino}pyrimidin-4-yl)benzamide

https://huagongshe.com/ko/reaction/31741

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물EthylenediamineHCID 3301—
반응물2-ChloropyridineHCID 7977—
반응물DiisopropylethylamineHCID 81531—
반응물N~1~-(Pyridin-2-yl)ethane-1,2-diamineHCID 410428—
반응물HCID 178512433HCID 178512433—
용매AcetonitrileHCID 6342—
생성물4-(2-{[2-(2-Pyridylamino)ethyl]amino}pyrimidin-4-yl)benzamideHCID 22142834—

반응 단계

2-(2-Aminoethylamino)pyridine (prepared from 2-chloropyridine and ethylenediamine in accordance with the method described in T. Mega et al., 1988, Bull. Chem. Soc. Japan 61:4315, which is incorporated herein by reference) (6 mmol) was treated with benzotriazole carboxamidinium 4-methylbenzenesulfonatesulfonate (2.0 g, 6 mmol) and DIEA (1.05 ml, 6 mmol) in anhydrous acetonitrile (10 ml) for 65 hours. Ether (ca. 10 ml) was then added to this mixture. After 8 hours the white solid amino[2-(2-pyridylamino)ethyl]carboxamidinium 4-methylbenzenesulfonate was filtered off and dried in vacuo. The resulting guanidine (200 mg) was reacted with 100 mg of resin (21 hours, 90° C.) according to the method described in Example 10 (Resin method C), to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425557B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-c5bdf6da68cb40abbb85507f429e9fe9
출처 메모uspto-grants-2008_09