Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389563Generated: October 31, 2026

2-Methyl-3-butyn-2-ol → 4-(3-Bromothieno[2,3-c]pyridin-2-yl)-2-methylbut-3-yn-2-ol

https://huagongshe.com/reaction/389563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-butyn-2-olHCID 8258—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,3-Dibromothieno[2,3-c]pyridineHCID 626220—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Product4-(3-Bromothieno[2,3-c]pyridin-2-yl)-2-methylbut-3-yn-2-olHCID 6676055787%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of 2,3-dibromothieno[2,3-c]pyridine (400 mg, 1.37 mmol), 2-methyl-3-butyn-2-ol (121 μL, 1.24 mmol), copper (I) iodide (24 mg, 0.12 mmol) and DIPEA (2.16 mL, 12.41 mmol) in 1,4-dioxane (16 mL) was added Pd(PPh3)2Cl2 (174 mg, 0.25 mmol). The mixture was evacuated and refilled with nitrogen (3×), then stirred at 50° C. for 2 h. Solvent was evaporated and the resultant mixture was dissolved in EtOAc. The organic solution was washed with water and brine, dried over anhydrous sodium sulfate, and purified by ISCO column chromatography (0 to 5% MeOH:DCM) to afford 319 mg (87%) of the title compound as a light-yellow solid. MS (ESI): 296.38, 298.35 [M+H]+; HPLC tR=0.94 min (HPLC: Analytical—2 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378104B2
Source datasetuspto-grants-2013_02
ORD IDord-99974af5f0bb46b18a072fdf9d645124
Source noteuspto-grants-2013_02