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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406072Generated: October 31, 2026

Pyridine → Methyl 3-((3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)benzyl)thio)propanoate

https://huagongshe.com/reaction/2406072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamideHCID 66587027—
ReactantMethyl 3-(3-(chlorocarbonyl)benzylthio)propanoateHCID 86705202—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-((3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)benzyl)thio)propanoateHCID 66587735—

Reaction Steps

To a solution of 2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide (138 mg, 0.37 mmol, 1.00 equiv) in tetrahydrofuran (6 mL) was added methyl 3-(3-(chlorocarbonyl)benzylthio)propanoate (112 mg, 0.41 mmol, 1.10 equiv) and pyridine (60 mg, 0.76 mmol, 2.00 equiv) and the resulting solution was stirred for 5 h at room temperature. The reaction progress was monitored by LCMS. The crude product was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809339B2
Source datasetuspto-grants-2014_08
ORD IDord-66280a5bcbb64bd49dc8232011e20201
Source noteuspto-grants-2014_08