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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501046Generated: November 1, 2026

Dichloromethane → 2-(6-Methylamino-3-pyridinyl)-1-benzofuran-5-ol

https://huagongshe.com/reaction/501046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(5-methoxy-1-benzofuran-2-yl)-N-methyl-2-pyridinamineHCID 25014927—
SolventWaterHCID 962—
Product2-(6-Methylamino-3-pyridinyl)-1-benzofuran-5-olHCID 2501484036.4%

Reaction Steps

[5-(5-Methoxy-benzofuran-2-yl)-pyridin-2-yl]-methylamine (0.24 mmol) was mixed with CH2Cl2 (3 mL) at 0° C. under argon atmosphere. BBr3 (1M in CH2Cl2) (1.0 mL, 1.0 mmol) was added dropwise and the mixture was stirred for 2 h at rt. The mixture was hydrolysed with H2O followed by NaHCO3 (sat. aq.) solution. The resulting mixture was extracted with EtOAc and the organic extracts were dried over Na2SO4. After filtration and evaporation of the solvent, the crude material was purified by preparative HPLC to afford the title compound as a white solid (21 mg). 1H NMR δ ppm 9.10 (s, 1 H) 8.50 (d, 1 H) 7.81 (dd, 1 H) 7.32 (d, 1 H) 6.96 (s, 1 H) 6.81-6.94 (m, 2 H) 6.66 (dd, 1 H) 6.54 (d, 1 H) 2.82 (d, 3 H); MS m/z 241 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772256B2
Source datasetuspto-grants-2010_08
ORD IDord-759231bec1b44933a1727ae892703e70
Source noteuspto-grants-2010_08