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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56241Generated: October 29, 2026

Triethyl orthoacetate → 3-((6-(2,4-dimethyl-6-oxopyrimidin-1(6H)-yl)-1H-indol-1-yl)methoxy)benzonitrile

https://huagongshe.com/reaction/56241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl orthoacetateHCID 66221—
ReactantHCID 90030960HCID 90030960—
Product3-((6-(2,4-dimethyl-6-oxopyrimidin-1(6H)-yl)-1H-indol-1-yl)methoxy)benzonitrileHCID 9003089625%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of (Z)-3-amino-N-(1-((3-cyanophenoxy)methyl)-1H-indol-6-yl)but-2-enamide (1.04 g, 3.00 mmol) and triethyl orthoacetate (20 mL) was stirred at 130° C. overnight. The mixture was cooled to rt and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (272 mg, 25%). The compound was characterized by the following spectroscopic data:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434695B2
Source datasetuspto-grants-2016_09
ORD IDord-fe15daea1c304f1d9d2d0f1f63da566c
Source noteuspto-grants-2016_09