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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69170Generated: October 28, 2026

1,2-Dimethoxyethane → 2-Chloro-4-(3-quinolin-6-ylmethyl-imidazo[1,2-b]pyridazin-6-yl)-benzamide

https://huagongshe.com/reaction/69170

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant(4-Carbamoyl-3-chlorophenyl)boronic acidHCID 44119639—
Reactant(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-quinolineHCID 44206294—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-Chloro-4-(3-quinolin-6-ylmethyl-imidazo[1,2-b]pyridazin-6-yl)-benzamideHCID 44206295—

Reaction Conditions

Temperature90 °C

Reaction Steps

A microwave tube was charged with (6-chloro-imidazo[1,2-b]pyridazin-3-yl)-quinoline (Example 14, 150 mg, 0.509 mmol), 4-carbamoyl-3-chlorophenyboronic acid (304 mg, 1.527 mmol), DME (1.6 mL) and DMF (250 μL). 2 M Na2CO3 (763 μL, 1.527 mmol) was then added, followed by tetrakis-(triphenylphosphine)-palladium (21 mg, 0.025 mmol). The RM was heated at 90° C. for 24 h. The cool reaction mixture was poured in DCM, filtered through a Celite pad and washed with water. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. While concentrating some crystals appeared. The crystals were filtered off and dried to afford the title compound as a beige solid (tR 4.28 min (conditions 4), MH+=414.4, 1H-NMR in DMSO-d6: 8.85 (m, 1H); 8.32 (m, 1H); 8.24 (d, 1H); 8.11 (m, 1H); 8.07 (dd, 1H); 7.97 (m, 3H); 7.86 (d, 1H); 7.80 (s, 1H); 7.78 (dd, 1H); 7.70 (s, 1H); 7.61 (d, 1H); 7.51 (dd, 1H); 4.63 (s, 2H)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-4c7e225ba3204cfe9d9da305fd0a5988
Source noteuspto-grants-2014_09