HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431587Generated: October 25, 2026
Potassium Phosphate, Tribasic → 2-(4-Methoxy-2,6-dimethylphenyl)-5-morpholinopyridin-3-amine
https://huagongshe.com/reaction/1431587
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | (2,6-Dimethyl-4-methoxyphenyl)boronic acid | HCID 3716303 | — |
| Reactant | 2-Chloro-5-morpholinopyridin-3-amine | HCID 59631039 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(4-Methoxy-2,6-dimethylphenyl)-5-morpholinopyridin-3-amine | HCID 59631164 | — |
Reaction Steps
2-Chloro-5-morpholinopyridin-3-amine (62 mg, 0.29 mmol), 4-methoxy-2,6-dimethylphenylboronic acid (0.07 g, 0.39 mmol), tricyclohexylphosphine (12 mg, 0.042 mmol), and tris(dibenzylideneacetone)dipalladium (0) (19 mg, 0.02 mmol) were added to a flask then degassed and backfilled with argon. To the flask, 1,4-dioxane (3 mL) and aq. 1.3M potassium phosphate tribasic (0.67 mL, 0.87 mmol) were added by syringe. The resulting reaction was heated to 90° C. and monitored with TLC and LC-MS. After 19 h, the reaction was cooled to rt then poured into water. After extracting twice with EtOAc and twice with DCM, the combined organic extractions were dried over anhydrous magnesium sulfate. After filtration and concentration, the residue was purified on silica gel (0-30% of a premixed solution of 89:9:1 DCM:MeOH:ammonium hydroxide in DCM) to afford a light yellow solid as 2-(4-methoxy-2,6-dimethylphenyl)-5-morpholinopyridin-3-amine. 1H NMR (500 MHz, CDCl3) δ ppm 7.75 (1H, br. s.), 6.75 (3H, m), 3.95 (4H, m), 3.85 (3H, m), 3.54 (2H, br. s.), 3.28 (4H, m), 2.04 (6H, s). Mass Spectrum (pos.) m/e: 314.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940724B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-08305a0d110c4588a5c3ba8bf9ba8859 |
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| Source note | uspto-grants-2015_01 |
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