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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351927Generated: October 26, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant2,2,2-Trichloroethyl pyridin-2-ylcarbamateHCID 11687642—
ReactantEthyl 3-phenyl-3-[6-(3-hydroxypropoxy)indol-3-yl]propionateHCID 15549282—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-phenyl-3-(6-{3-[(pyridin-2-yl)(2,2,2-trichloroethoxycarbonyl) amino]propoxy}indol-3-yl)propionateHCID 15549283—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743810B2
Source datasetuspto-grants-2004_06
ORD IDord-6368bd859e1d47f7bc07fce48a640c73
Source noteuspto-grants-2004_06