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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386140Generated: October 30, 2026

Potassium Carbonate → 5-{[tert-Butyl(dimethyl)silyl]ethynyl}-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamide

https://huagongshe.com/reaction/386140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant4-((6-Bromopyridin-2-yl)methyl)morpholineHCID 23438147—
Reactant2-Amino-5-{[tert-butyl(dimethyl)silyl]ethynyl}thiophene-3-carboxamideHCID 59526335—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product5-{[tert-Butyl(dimethyl)silyl]ethynyl}-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamideHCID 59526210—

Reaction Conditions

Temperature100 °C

Reaction Steps

4-[(6-Bromopyridin-2-yl)methyl]morpholine (Example 45, Step 1) (340 mg, 1.32 mmol), 2-amino-5-{[tert-butyl(dimethyl)silyl]ethynyl}thiophene-3-carboxamide (445 mg, 1.59 mmol), Pd2dba3 (121 mg, 0.13 mmol), X-Phos (315 mg, 0.66 mmol), and K2CO3 (201 mg, 1.46 mmol) were combined in a vial, sealed, and evacuated/backfilled with nitrogen. Degassed t-amyl alcohol (3.3 ml), and the reaction was vigorously stirred at 100° C. overnight. The reaction mixture was then diluted with MeOH, combined with silica, and evaporated. Flash chromatography (dry load, 0-10% MeOH/EtOAc) afforded the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-c13545f2cc474191a87ad7a0a154d458
Source noteuspto-grants-2013_02