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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502217Generated: November 1, 2026

Potassium Phosphate, Tribasic → Benzyl 4-(3-{[3-(2-tert-butoxy-2-oxoethyl)-2,4-dioxo-1,2,3,4-tetrahydroquinazolin-7-yl]carbonyl}-2-methylindolizin-1-yl)benzoate

https://huagongshe.com/reaction/1502217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPotassium bisulfateHCID 516920—
Reactant4-(Benzyloxycarbonyl)phenylboronic AcidHCID 2773251—
Reactanttert-butyl {7-[(1-bromo-2-methylindolizin-3-yl)carbonyl]-2,4-dioxo-1,4-dihydroquinazolin-3(2H)-yl}acetateHCID 131734308—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-(3-{[3-(2-tert-butoxy-2-oxoethyl)-2,4-dioxo-1,2,3,4-tetrahydroquinazolin-7-yl]carbonyl}-2-methylindolizin-1-yl)benzoateHCID 8965767092%

Reaction Conditions

Temperature80 °C

Reaction Steps

{4-[(Benzyloxy)carbonyl]phenyl}boronic acid (0.7 g, 2.73 mmol), 5.5 mL of a molar solution of potassium phosphate and the catalyst PdCl2(dppf) (192 mg, 0.27 mmol) are added to a solution of tert-butyl {7-[(1-bromo-2-methylindolizin-3-yl)carbonyl]-2,4-dioxo-1,4-dihydroquinazolin-3(2H)-yl}acetate [described in Step 3.2.] (1 g, 1.82 mmol) in 20 mL of DMF placed in a microwave reactor under nitrogen. The reactor is sealed and the solution is heated for 30 min at 80° C. in a microwave. The reaction medium is cooled and run into a molar solution of KHSO4, and extracted with EtOAc. The organic phase is washed with a saturated aqueous solution of NaCl, dried over Na2SO4, and concentrated to dryness. The residue obtained is purified by flash chromatography on silica (DCM/EtOH: 100/0 to 80/20] to give 1.08 mg (92%) of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206177B2
Source datasetuspto-grants-2015_12
ORD IDord-58194a709d4a4c1392cb8275620f643f
Source noteuspto-grants-2015_12