Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631475Generated: November 4, 2026

Trifluoroacetic acid → HCID 11566711, compound

https://huagongshe.com/reaction/1631475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 67218912HCID 67218912—
ReactantHCID 67219373HCID 67219373—
ProductHCID 11566711HCID 11566711—

Reaction Steps

(2-Ethyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-acetic acid methyl ester: To a solution of triethylsilane (818 μl, 5.12 mmol) in TFA (1.6 ml) at −10° C. is added portion wise (2-ethyl-1 H-pyrrolo[2,3-b]pyridin-3-yl)-oxo-acetic acid methyl ester (0.34 g, 1.46 mmol). After stirring at room temperature overnight, the solvent is removed in vacuo and the resulting residue is neutralized with saturated sodium bicarbonate solution. The solution is extracted with DCM (3×20 ml) and the organic portions are combined, dried (Na2SO4) and concentrated in vacuo. The residue is loaded on a pre-packed Isolute™ silica column and eluted with DCM/MeOH (100:0 increasing to 98:2) to yield the titled compound as a yellow powder. (MH+ 219)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791256B2
Source datasetuspto-grants-2014_07
ORD IDord-6eed2c19342c4fd182eba30f5238f061
Source noteuspto-grants-2014_07