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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853041Generated: October 31, 2026

Potassium Phosphate, Tribasic → 4-(4-(5-(Methylthio)imidazo[1,2-c]pyrimidin-7-yl)phenyl)morpholine

https://huagongshe.com/reaction/1853041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(4-(Morpholin-4-yl)phenyl)boronic acidHCID 2795359—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant7-Chloro-5-(methylthio)imidazo[1,2-c]pyrimidine hydrochlorideHCID 86685296—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventIsopropanolHCID 3776—
Product4-(4-(5-(Methylthio)imidazo[1,2-c]pyrimidin-7-yl)phenyl)morpholineHCID 6745769125.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

A suspension of 7-chloro-5-(methylthio)imidazo[1,2-c]pyrimidine hydrochloride (1.85 g, 7.83 mmol; Preparation H, Step A), 4-morpholinophenylboronic acid (1.78 g, 8.62 mmol) and potassium phosphate (3.33 g, 15.7 mmol) in isopropanol (25 mL) was purged with argon for 5 minutes, and then Pd2dba3 (0.717 g, 0.783 mmol) and XPHOS (1.49 g, 3.13 mmol) were added. The reaction was again purged for 5 minutes with argon before being sealed and heated to 90° C. for 18 hours. The reaction mixture was diluted with EtOAc (75 mL) and filtered. The filtrate was concentrated under reduced pressure, and the residue obtained was purified by silica gel column chromatography, eluting with 10-15-20% acetone in DCM to afford 4-(4-(5-(methylthio)imidazo[1,2-c]pyrimidin-7-yl)phenyl)morpholine (0.663 g, 25.9% yield) as a yellow solid. MS (apci) m/z=327.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962596B2
Source datasetuspto-grants-2015_02
ORD IDord-8950542511ea4a74b1e3e701b44305a4
Source noteuspto-grants-2015_02