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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870623Generated: November 2, 2026

Potassium Phosphate, Tribasic → 3-(4-(aminomethyl)phenyl)-N-(2-methoxyethyl)imidazo[1,2-b]pyridazin-6-amine mono acetic acid salt

https://huagongshe.com/reaction/870623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(4-(Aminomethyl)phenyl)boronic acidHCID 2734312—
Reactant3-bromo-N-(2-methoxyethyl)imidazo[1,2-b]pyridazin-6-amineHCID 57470622—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
Product3-(4-(aminomethyl)phenyl)-N-(2-methoxyethyl)imidazo[1,2-b]pyridazin-6-amine mono acetic acid saltHCID 86696320—

Reaction Conditions

Temperature160 °C

Reaction Steps

To a mixture of 3-bromo-N-(2-methoxyethyl)imidazo[1,2-b]pyridazin-6-amine (229 mg, 0.85 mmol), (4-(aminomethyl)phenyl)boronic acid (395 mg, 2.11 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (62 mg, 0.085 mmol) and potassium phosphate (540 mg, 2.54 mmol) was added 1:1 Dimethoxyethane/water (3 mL). The resulting mixture was heated at 160° C. (microwave) for 6 min. The reaction was then filtered and diluted with a mixture of 1:1:1 methanol/water/acetonitrile, and then filtered again. The filtration was finally purified by preparative HPLC (acidic) to afford 3-(4-(aminomethyl)phenyl)-N-(2-methoxyethyl)imidazo[1,2-b]pyridazin-6-amine mono acetic acid salt as a white solid: 1H NMR (METHANOL-d4) δ: 8.18-8.33 (m, J=8.3 Hz, 2H), 7.82 (s, 1H), 7.67 (d, J=9.6 Hz, 1H), 7.53-7.58 (m, J=8.3 Hz, 2H), 6.78 (d, J=9.6 Hz, 1H), 4.14 (s, 2H), 3.68 (t, J=5.7 Hz, 2H), 3.58 (t, J=5.4 Hz, 2H), 3.42 (s, 3H), 1.93 (s, 3H); LRMS (ESI) m/e 298.2 [(M+H)+, calcd for C16H20N5O 298.2]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969565B2
Source datasetuspto-grants-2015_03
ORD IDord-6d32a3fbea86499ca7f0cc925e3dc6e2
Source noteuspto-grants-2015_03