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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028035Generated: October 27, 2026

Tributylphosphine → Ethyl 5-fluoro-1-[2-(pyridin-3-yl)ethyl]-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1028035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant3-PyridineethanolHCID 80515—
Reactantethyl 5-fluoro-1H-indole-2-carboxylateHCID 2727899—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-fluoro-1-[2-(pyridin-3-yl)ethyl]-1H-indole-2-carboxylateHCID 1597898041.3%

Reaction Steps

A solution of 0.365 g (1.44 mmol) of 1,1′-(azodicarbonyl)dipiperidine in 10 ml of tetrahydrofuran is added dropwise to a solution of 0.2 g (0.97 mmol) of ethyl 5-fluoro-1H-indole-2-carboxylate, 0.178 g (1.45 mmol) of 2-(pyrid-3-yl)ethanol and 0.36 ml (1.44 mmol) of tributylphosphine in 30 ml of tetrahydrofuran. The reaction mixture is stirred overnight at room temperature and then concentrated under reduced pressure and taken up in 50 ml of cyclohexane. The suspension is then filtered and the filtrate is chromatographed on a column of silica (eluent: dichloromethane/methanol). 0.125 g of the expected product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735432B2
Source datasetuspto-grants-2014_05
ORD IDord-67c50f2d0a5c4efa86d731eef8274961
Source noteuspto-grants-2014_05