Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386141Generated: October 26, 2026

Tetrabutylammonium Fluoride → 5-Ethynyl-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamide

https://huagongshe.com/reaction/386141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-{[tert-Butyl(dimethyl)silyl]ethynyl}-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamideHCID 59526210—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Ethynyl-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamideHCID 59526270—

Reaction Steps

To a solution of 5-{[tert-butyl(dimethyl)silyl]ethynyl}-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamide (435 mg, 0.95 mmol) in THF (15 mL) was added TBAF (1.0 M in THF, 2.38 mL, 2.38 mmol), and the reaction was stirred at room temperature for 6 h. The solution was diluted with water and extracted with EtOAc (2×). The organic extracts were dried over magnesium sulfate, filtered, combined with silica gel and evaporated. Flash chromatography (dry load, 0-10% MeOH/EtOAc) provided the title compound as a gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-485d6586e8ec40e4a8dbe538bd9a1877
Source noteuspto-grants-2013_02