Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401711Generated: October 31, 2026

Potassium Phosphate, Tribasic → 1-tert-Butyl 6-methyl 3-phenyl-1H-indole-1,6-dicarboxylate

https://huagongshe.com/reaction/401711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-tert-butyl 6-methyl 3-iodo-1H-indole-1,6-dicarboxylateHCID 7127827—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant1-{1-[(4-Cyclohexylphenyl)carbonyl]azetidin-3-yl}-4-(phenylcarbonyl)-piperazineHCID 49763155—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product1-tert-Butyl 6-methyl 3-phenyl-1H-indole-1,6-dicarboxylateHCID 59626044—

Reaction Steps

A mixture of 1-tert-butyl 6-methyl 3-iodo-1H-indole-1,6-dicarboxylate 62a (5.02 mmol, 2.016 g), phenylboronic acid 1× (7.53 mmol, 0.92 g), Pd(OAc)2 (0.402 mmol, 90 mg), Sphos 0.904 mmol, (0.37 g), and K3PO4 (10.1 mmol, 2.13 g) in toluene (10 mL) in sealed reaction vial was stirred at room temperature for 2 min and then heated at 90° C. under N2 for 4 h. The reaction mixture was quenched with EtOAc and water. The organic layer was concentrated and purified by flash column chromatography (silica gel, 8% EtOAc/hexanes). The desired product was collected as a light yellow solid that was washed with small amount of hexanes to obtain 62b as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741887B2
Source datasetuspto-grants-2014_06
ORD IDord-94dfe094f7244aa3b05880cb85ffedc7
Source noteuspto-grants-2014_06