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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661135Generated: October 30, 2026

3,4-Dihydro-2H-1,4-benzoxazine → 4-[3-(dipyridin-3-ylmethoxy)pyridin-2-yl]-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/1661135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dihydro-2H-1,4-benzoxazineHCID 585096—
ReactantSodium t-butoxideHCID 23676156—
Reactant2-Bromo-3-(dipyridin-3-ylmethoxy)pyridineHCID 57613256—
CatalystHCID 178418851HCID 178418851—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-[3-(dipyridin-3-ylmethoxy)pyridin-2-yl]-3,4-dihydro-2H-1,4-benzoxazineHCID 24760404—

Reaction Steps

To a solution of 2-bromo-3-(dipyridin-3-ylmethoxy)pyridine (150 mg, 0.438 mmol) and 3,4-dihydro-2H-1,4-benzoxazine (59 mg, 0-438 mmol) in dry dioxane (5 mL) was added sodium t-butoxide (63 mg, 0.658 mmol), bis(tri-t-butylphosphine)palladium(0) (22 mg, 0.044 mmol). The mixture was heated to 100 C for 6 h. The reaction was cooled, diluted with water and extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, filtered, and the solvent evaporated. The residue was purified by silica gel chromatography (3-5% MeOH in CH2Cl2) to give 4-[3-(dipyridin-3-ylmethoxy)pyridin-2-yl]-3,4-dihydro-2H-1,4-benzoxazine (2-3). LRMS m/z (M+H) Calcd: 397.5, found: 397.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030332B2
Source datasetuspto-grants-2011_10
ORD IDord-d07fc83a69804071ad984b97b48483a9
Source noteuspto-grants-2011_10