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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778827Generated: November 4, 2026

4,4,5,5-Tetramethyl[1,3,2]dioxaborolane → tert-butyl 6-(8-(benzo[d]thiazol2-ylcarbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinate

https://huagongshe.com/reaction/1778827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
Reactant1,1-Dimethylethyl 6-(8-((2-benzothiazolylamino)carbonyl)-3,4-dihydro-2(1H)-isoquinolinyl)-3-bromo-2-pyridinecarboxylateHCID 59447615—
CatalystHCID 178418807HCID 178418807—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Producttert-butyl 6-(8-(benzo[d]thiazol2-ylcarbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinateHCID 89498009—

Reaction Steps

A mixture of EXAMPLE 1D (1.2 g), 1.0 M 4,4,5,5-tetramethyl-1,3,2-dioxaborolane in tetrahydrofuran (4.24 mL), triethylamine (0.92 mL), and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane (0.087 g) in CH3CN (15 mL) was heated at 100° C. in a Biotage Initiator microwave reactor for 30 minutes. After cooling, the reaction mixture was partitioned between water and ethyl acetate. The organic layer was extracted with additional ethyl acetate twice. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was purified by flash column chromatography on silica gel to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266877B2
Source datasetuspto-grants-2016_02
ORD IDord-2d93d92f92a3462bb4769ee861830935
Source noteuspto-grants-2016_02