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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | (4-(Morpholin-4-yl)phenyl)boronic acid | HCID 2795359 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 7-Chloro-5-(methylthio)imidazo[1,2-c]pyrimidine hydrochloride | HCID 86685296 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(4-(5-(Methylthio)imidazo[1,2-c]pyrimidin-7-yl)phenyl)morpholine | HCID 67457691 | 25.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962596B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-8950542511ea4a74b1e3e701b44305a4 |
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| Source note | uspto-grants-2015_02 |
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