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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627310Generated: October 29, 2026

Triethylamine → [6-(5-Ethoxymethoxy-benzofuran-2-yl)-2-nitro-pyridin-3-yl]-methyl-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/627310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Ethoxymethoxy-benzofuran-2-boronic acidHCID 46183970—
Reactant(6-Bromo-2-nitro-pyridin-3-yl)-methyl-carbamic acid tert-butyl esterHCID 46855854—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
Product[6-(5-Ethoxymethoxy-benzofuran-2-yl)-2-nitro-pyridin-3-yl]-methyl-carbamic acid tert-butyl esterHCID 4618396984.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a degassed solution of 5-ethoxymethoxy-benzofuran boronic acid (4) (140 mg, 0.593 mmol) in ethanol (10 mL), (6-bromo-2-nitro-pyridin-3-yl)-methyl-carbamic acid tert-butyl ester (7) (151 mg, 0.455 mmol), Pd(PPh3)2Cl2 (42 mg, 0.059 mmol) and Et3N (127 μL, 0.909 mmol) were added. The reaction mixture was stirred at 100° C. for 30 minutes in a microwave reactor. Volatiles were removed under reduced pressure. The residue was diluted with water (15 mL) and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with water, brine, dried over Na2SO4, and concentrated under reduced pressure. The crude product was purified by flash column chromatography using 20% ethyl acetate in hexane. Evaporation of solvent gave title compound 8 (170 mg) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309267B2
Source datasetuspto-grants-2016_04
ORD IDord-94bcb6ea5bce452994c3e6d7a15c6332
Source noteuspto-grants-2016_04