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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046407Generated: October 26, 2026

Triethylamine → HCID 58046440, compound

https://huagongshe.com/reaction/2046407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
ReactantMethyl 5-bromo-4-(imidazo[1,2-b]pyridazin-3-yl)thiophene-2-carboxylateHCID 58046405—
CatalystHCID 178418807HCID 178418807—
Solvent1-PropanolHCID 1031—
ProductHCID 58046440HCID 58046440—

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl-5-bromo-4-(imidazo[1,2-b]pyridazin-3-yl)thiophene-2-carboxylate (200 mg, 0.591 mmol), potassium vinyltrifluoroborate (119 mg, 0.887 mmol), PdCl2(dppf)-CH2Cl2 adduct (48 mg, 0.059 mmol), and triethylamine (0.165 mL, 1.18 mmol) was dissolved in n-propanol (5.91 mL) and purged with nitrogen for 5 minutes in a sealed tube. The solution was heated at 100° C. for 18 h. the reaction was cooled to room temperature and quenched with saturated sodium bicarbonate. The aqueous layer was extracted with ethyl acetate (×3) and the organic layers combined, dried with magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography to afford the title compound as an orange solid. 1H NMR (500 MHz, CD3SOCD3) δ 8.61 (d, 1H); 8.23 (d, 1H); 8.16 (s, 1H); 7.95 (s, 1H); 7.32 (dd, 1H); 6.94 (dd, 1H); 5.87 (d, 1H); 5.44 (d, 1H); 3.85 (s, 3H). LRMS (APCI) calc'd for (C14H11N3O2S) [M+11]+, 286.1. found 286.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592425B2
Source datasetuspto-grants-2013_11
ORD IDord-0380dd10f42642c48eda19af5f695715
Source noteuspto-grants-2013_11