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HRID 351927생성일: 2026년 10월 26일

Triphenylphosphine → Ethyl 3-phenyl-3-(6-{3-[(pyridin-2-yl)(2,2,2-trichloroethoxycarbonyl) amino]propoxy}indol-3-yl)propionate

https://huagongshe.com/reaction/351927

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물2,2,2-Trichloroethyl pyridin-2-ylcarbamateHCID 11687642—
반응물Ethyl 3-phenyl-3-[6-(3-hydroxypropoxy)indol-3-yl]propionateHCID 15549282—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-phenyl-3-(6-{3-[(pyridin-2-yl)(2,2,2-trichloroethoxycarbonyl) amino]propoxy}indol-3-yl)propionateHCID 15549283—

반응 단계

500 mg (1.36 mmol) of 5 and 550 mg (2.04 mmol) of 2-(2,2,2-trichloroethoxycarbonylamino)pyridine and 907 mg (2.72 mmol) of triphenylphosphine (polymer-bound) are introduced into 7.5 ml of anhydrous THF, and a solution of 0.32 ml (2.04 mmol) of azodicarboxylic acid diethyl ester (diethyl azodicarboxylate, DEAD) in 7.5 ml of THF is added dropwise at room temperature over the course of 30 minutes. The TLC check shows complete conversion after 1.5 hours. The polymer is filtered off, and the solution is washed with a little water, dried and evaporated. The residue can be purified by chromatography on silica gel (eluent gradient toluene/acetone 20:1→4:1), giving ethyl 3-phenyl-3-(6-{3-[(pyridin-2-yl)(2,2,2-trichloroethoxycarbonyl)amino]propoxy}indol-3-yl)propionate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743810B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-6368bd859e1d47f7bc07fce48a640c73
출처 메모uspto-grants-2004_06