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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423846Generated: November 2, 2026

Potassium Carbonate → 7-(((5-Bromo-4-chloro-2-nitrophenyl)amino)methyl)-3-neopentyl-1-oxa-3-azaspiro[4.5]decan-2-one

https://huagongshe.com/reaction/1423846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-2-chloro-5-fluoro-4-nitrobenzeneHCID 10400105—
Reactant7-(Aminomethyl)-3-neopentyl-1-oxa-3-azaspiro[4.5]decan-2-oneHCID 71116056—
SolventAcetonitrileHCID 6342—
Product7-(((5-Bromo-4-chloro-2-nitrophenyl)amino)methyl)-3-neopentyl-1-oxa-3-azaspiro[4.5]decan-2-oneHCID 7111604544.3%

Reaction Steps

A rt suspension of 1-bromo-2-chloro-5-fluoro-4-nitrobenzene (0.600 g, 2.36 mmol) in MeCN (8 mL) was treated with 7-(aminomethyl)-3-neopentyl-1-oxa-3-azaspiro[4.5]decan-2-one (0.400 g, 1.57 mmol) and potassium carbonate (0.543 g, 3.93 mmol). The reaction was stirred for 18 h, and the solids were filtered off and washed with EtOAc. The filtrate was concentrated and purified on a 40 g silica gel column (0-100% DCM/hexanes, 20 min gradient; 100% DCM, 15 min; 40 mL/min elution; 254 nm detection) to provide the title compound (0.340 g, 44% yield) as an orange solid. MS (m/z) 488.1, 490.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927585B2
Source datasetuspto-grants-2015_01
ORD IDord-55a0e8fc57a746bf90ed4f2b1bb84814
Source noteuspto-grants-2015_01