Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870632Generated: November 1, 2026

1,2-Dimethoxyethane → HCID 86696327, compound

https://huagongshe.com/reaction/870632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Aminomethylphenylboronic acid hydrochlorideHCID 2734311—
ReactantHCID 66889019HCID 66889019—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
ProductHCID 86696327HCID 8669632744%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 3-bromo-N-cyclohexylimidazo[1,2-b]pyridazin-6-amine (100 mg, 0.34 mmol), 4-(aminomethyl)phenylboronic acid hydrochloride (160 mg, 0.84 mmol), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloromethane adduct (25 mg, 0.034 mmol), potassium phosphate (360 mg, 1.7 mmol), DME (1.5 mL) and H2O (0.5 mL) was heated in a sealed conical vessel at 160° C. for 360 s by microwave irradiation. The organic layer was separated and the aqueous layer was extracted with ethyl acetate (2 mL). The combined organic layers were concentrated under reduced pressure to afford an oil that was purified by reverse phase HPLC to afford [3-(4-aminomethyl-phenyl)-imidazo[1,2-b]pyridazin-6-yl]-cyclohexylamine (48 mg, 44%) as a white solid: 1H NMR (400 MHz, MeOD-d4) δ ppm 8.29 (d, J=8.6 Hz, 2H), 7.82 (s, 1H), 7.63 (d, J=9.6 Hz, 1H), 7.54 (d, J=8.6 Hz, 2H), 6.72 (d, J=9.6 Hz, 1H), 4.13 (s, 2H), 3.70-3.78 (m, 1H), 2.19 (d, J=9.1 Hz, 2H), 1.83-1.93 (m, 2H), 1.70-1.76 (m, 1H), 1.42-1.54 (m, 2H), 1.29-1.40 (m, 3H); LCMS (ESI) m/e 322.2 [(M+H)+, calcd for C19H24N5 322.2].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969565B2
Source datasetuspto-grants-2015_03
ORD IDord-be5a218086cd491e9ea5c40663a29262
Source noteuspto-grants-2015_03