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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593148Generated: October 29, 2026

1,4-Dioxane → 3-Amino-5-bromo-1-methyl-1,2-dihydropyridin-2-one

https://huagongshe.com/reaction/593148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant5-bromo-3-(diphenylmethyleneamino)-1-methylpyridin-2(1H)-oneHCID 86684584—
SolventEthyl AcetateHCID 8857—
Product3-Amino-5-bromo-1-methyl-1,2-dihydropyridin-2-oneHCID 5291126852.1%

Reaction Steps

To a solution of 5-bromo-3-(diphenylmethyleneamino)-1-methylpyridin-2(1H)-one (3.82 g, 10.4 mmol) in ethyl acetate (10 mL) was added 4 MHCl/dioxane (7.8 mL, 31.3 mmol). The reaction mixture was stirred for 0.5 h and concentrated under reduced pressure. The residue was washed with tert-butyl methyl ether and filtered. The solid was dissolved in ethyl acetate (10 mL) and water (10 mL). The pH of the resulting mixture was adjusted to between 7 and 8 by adding K2CO3 gradually. The water phase was separated and extracted with dichloromethane for three times. The combined organic layer was concentrated under reduced pressure to afford 325a as a yellow solid (1.1 g, 52%). MS-ESI: [M+H]+ 202.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238655B2
Source datasetuspto-grants-2016_01
ORD IDord-9ff511ce15504abbb20a28f791ce8a61
Source noteuspto-grants-2016_01