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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241808Generated: November 1, 2026

Boron tribromide → 2-[6-(Dimethylamino)pyridin-3-yl]-1,3-benzoxazol-5-ol

https://huagongshe.com/reaction/2241808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(5-methoxy-1,3-benzoxazol-2-yl)-N,N-dimethylpyridin-2-amineHCID 24780656—
SolventDichloromethaneHCID 6344—
Product2-[6-(Dimethylamino)pyridin-3-yl]-1,3-benzoxazol-5-olHCID 2478065723.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-(5-methoxy-1,3-benzoxazol-2-yl)-N,N-dimethylpyridin-2-amine (0.368 mmol) in dichloromethane (2.0 mL) was added BBr3 in dichloromethane (1.84 mmol) at 0° C. under an atmosphere of argon and the reaction stirred for 1 h at 0° C. The reaction mixture was neutralized with NaHCO3 (sat. aq.) and dichloromethane was added. The layers were separated and the aqueous phase was extracted with dichloromethane (4×). The combined organic phases were dried (MgSO4), filtered and the solvents removed in vacuo. The crude material was purified by preparative HPLC to give 22.3 mg of the title compound as a white solid. 1H NMR δ ppm 9.44 (s, 1H), 8.83 (d, 1H), 8.13 (dd, 1H), 7.48 (d, 1H), 7.01 (d, 1H), 6.80 (d, 1H), 6.76 (dd, 1H), 3.14 (s, 6H). MS m/z (M+H) 256.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07670591B2
Source datasetuspto-grants-2010_03
ORD IDord-52538839318447f79a7015f49c633089
Source noteuspto-grants-2010_03