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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535446Generated: October 30, 2026

3-(Methoxycarbonyl)benzeneboronic acid → Methyl 2-amino-5-({1-[3-(methoxycarbonyl)phenyl]-2-methylindolizin-3-yl}carbonyl)benzoate

https://huagongshe.com/reaction/535446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methoxycarbonyl)benzeneboronic acidHCID 2734714—
ReactantPotassium phosphate dihydrateHCID 23436936—
ReactantMethyl 2-amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoateHCID 57500395—
CatalystHCID 178418397HCID 178418397—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
ProductMethyl 2-amino-5-({1-[3-(methoxycarbonyl)phenyl]-2-methylindolizin-3-yl}carbonyl)benzoateHCID 6665315365.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

0.229 g (1.27 mmol) of [3-(methoxycarbonyl)phenyl]boronic acid, 0.492 g (2.12 mmol) of potassium phosphate dihydrate and 0.024 g (0.02 mmol) of tetrakis(triphenylphosphine)palladium are added, under an argon atmosphere at ambient temperature, to 0.410 g (1.06 mmol) of methyl 2-amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoate in 8 ml of a DME/H2O (5/1) mixture. The reaction medium is heated at 90° C. for 18 hours. The reaction medium is extracted with dichloromethane, washed with a saturated aqueous solution of sodium chloride, dried over sodium sulphate, filtered, and then concentrated under reduced pressure. The solid obtained is purified by silica gel column chromatography, elution being carried out with dichloromethane. 309 mg of a yellow solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859544B2
Source datasetuspto-grants-2014_10
ORD IDord-ca3aab6099ff4c8bba625c3ea634d623
Source noteuspto-grants-2014_10