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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506201Generated: October 25, 2026

2-[3-(2-Methoxyethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → HCID 68465011, compound

https://huagongshe.com/reaction/506201

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[3-(2-Methoxyethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 59558740—
Reactant5-iodo-4-[(4-methyl-1H-indol-5-yl)amino]nicotinonitrileHCID 68443831—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium BicarbonateHCID 516892—
ProductHCID 68465011HCID 6846501166%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 5-iodo-4[(4-methyl-1H-indol-5-yl)amino]nicotinonitrile (100 mg, 0.27 mmol), 2-[3-(2-methoxyethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (98 mg, 0.35 mmol) and tetrakis(triphenylphosphine)palladium(0) (16 mg, 0.014 mmol) in DME (6 mL) and saturated aqueous NaHCO3 (4 mL) was heated at 95° C. for 2 h, cooled to room temperature and partitioned between dichloromethane and water. The organic phase was dried over Na2SO4, filtered, and concentrated in vacuo, and the residue was purified by flash column chromatography (MeOH/CH2Cl2, 1% to 5%) to provide 71 mg (66%) of 5-[3-(2-methoxyethoxy)phenyl]-4-[(4-methyl-1H-indol-5-yl)amino]nicotinonitrile as a tan solid. HPLC retention time: 8.3 min.(g); MS: 399.3 (M+H); melting range: 158-160° C.; and HRMS: 399.18291.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781591B2
Source datasetuspto-grants-2010_08
ORD IDord-b2c8ac49a46340b786b41390b92fa431
Source noteuspto-grants-2010_08