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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227141Generated: October 30, 2026

Dimethylformamide → 1-(6-Amino-pyridin-2-ylmethyl)-3-(2,3-dihydro-benzo[1,4]dioxine-6-carbonyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/227141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant3-(2,3-Dihydro-benzo[1,4]dioxine-6-carbonyl)-1H-quinolin-4-oneHCID 57754543—
ReactantN-[1-(2-Bromo-1-methyl-ethylideneamino)-vinyl]-2,2,2-trifluoro-acetamideHCID 86613650—
Product1-(6-Amino-pyridin-2-ylmethyl)-3-(2,3-dihydro-benzo[1,4]dioxine-6-carbonyl)-1H-quinolin-4-oneHCID 57754731—

Reaction Steps

The mixture of 3-(2,3-Dihydro-benzo[1,4]dioxine-6-carbonyl)-1H-quinolin-4-one 70 mg (0.228 mmol) in DMF (1 mL) and sodium hydride 11.8 mg (0.296 mmol ) was stirred at room temperature for 60 min, followed by the addition of N-[1-(2-Bromo-1-methyl-ethylideneamino)-vinyl]-2,2,2-trifluoro-acetamide 83.8 mg (0.296 mmol). The mixture was stirred for 60 min, quenched with water, taken up with ethyl acetate, dried over sodium sulfate and purified with flash chromatography. The purified product was treated with Diethylamine in methanol over weekend, filtered to give the desired product 10 mg. LCMS observed for (M+H)+: 414.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-b510273cbc914de985461e85875d6ba7
Source noteuspto-grants-2009_07