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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051215Generated: November 4, 2026

Water → [2-(4-chloro-2-methoxy-pyridin-3-yl)-1H-indol-6-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1051215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant{4-[(E)-2-(4-chloro-2-methoxy-pyridin-3-yl)-vinyl]-3-nitro-phenyl}-carbamic acid tert-butyl esterHCID 90102932—
SolventTriethyl phosphiteHCID 31215—
Product[2-(4-chloro-2-methoxy-pyridin-3-yl)-1H-indol-6-yl]-carbamic acid tert-butyl esterHCID 9010292033%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of {4-[(E)-2-(4-chloro-2-methoxy-pyridin-3-yl)-vinyl]-3-nitro-phenyl}-carbamic acid tert-butyl ester (800 mg, 1.97 mmol) in triethyl phosphite (16.0 ml) was refluxed for 3 hours. The reaction mixture was cooled to 25° C., and poured into water. The aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed with brine and dried over magnesium sulfate. Filtration followed by concentration in vacuo gave a brown solid. Flash chromatography (70/30 hexanes/ethyl acetate) afforded [2-(4-chloro-2-methoxy-pyridin-3-yl)-1H-indol-6-yl]-carbamic acid tert-butyl ester (180 mg, 33%) as a white solid. MH+ 374.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388166B2
Source datasetuspto-grants-2016_07
ORD IDord-173a6a15a00f414892a11a05646dfef6
Source noteuspto-grants-2016_07