HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870632Generated: November 1, 2026
1,2-Dimethoxyethane → HCID 86696327, compound
https://huagongshe.com/reaction/870632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 4-Aminomethylphenylboronic acid hydrochloride | HCID 2734311 | — |
| Reactant | HCID 66889019 | HCID 66889019 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86696327 | HCID 86696327 | 44% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969565B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-be5a218086cd491e9ea5c40663a29262 |
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| Source note | uspto-grants-2015_03 |
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