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HRID 351927作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物2,2,2-Trichloroethyl pyridin-2-ylcarbamateHCID 11687642—
反応物Ethyl 3-phenyl-3-[6-(3-hydroxypropoxy)indol-3-yl]propionateHCID 15549282—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-phenyl-3-(6-{3-[(pyridin-2-yl)(2,2,2-trichloroethoxycarbonyl) amino]propoxy}indol-3-yl)propionateHCID 15549283—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06743810B2
出典データセットuspto-grants-2004_06
ORD IDord-6368bd859e1d47f7bc07fce48a640c73
出典メモuspto-grants-2004_06