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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541741Generated: October 31, 2026

Potassium Carbonate → Methyl 3-(2-{3-[(tert-butoxycarbonyl)amino]phenyl}ethyl)-5-[(2,5-dichloropyrimidin-4-yl)amino]benzoate

https://huagongshe.com/reaction/541741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,4,5-TrichloropyrimidineHCID 237259—
ReactantMethyl 3-amino-5-(2-{3-[(tert-butoxycarbonyl)amino]phenyl}ethyl)benzoateHCID 57961977—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(2-{3-[(tert-butoxycarbonyl)amino]phenyl}ethyl)-5-[(2,5-dichloropyrimidin-4-yl)amino]benzoateHCID 5796202772%

Reaction Steps

A solution of 2,4,5-trichloropyrimidine (0.371 mL, 3.24 mmol) and methyl 3-amino-5-(2-{3-[(tert-butoxycarbonyl)amino]phenyl}ethyl)benzoate (1.20 g, 3.24 mmol) in DMF (20 mL) and potassium carbonate (895 mg, 6.48 mmol) were stirred at 60° C. overnight. The reaction mixture was diluted with 1 N HCl and extracted with ethyl acetate three times. The combined organic solutions were dried with sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by flash column chromatography to yield the desired product (1.20 g, 72%). LCMS for C25H26Cl2N4O4Na (M+Na)+: m/z=539.3, 541.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-dd60adeda7de45caa2b2a12d3987e532
Source noteuspto-grants-2014_10