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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39414Generated: October 29, 2026

N,N'-Dimethylethylenediamine → N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide

https://huagongshe.com/reaction/39414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamideHCID 46928351—
Reactant5-Bromo-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthaleneHCID 53492696—
ProductN-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamideHCID 53491464—

Reaction Steps

A 20 ml screw-cap vial was filled with the following solids: CuO (0.05 mmol, 4.0 mg), anhydrous CuCl2 (0.05 mmol, 6.7 mg), K2CO3 (2.0 mmol, 277 mg), 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid amide (1.1 mmol, 193 mg) and 5-bromo-9-dichloromethylene-1,2,3,4-tetrahydro-1,4-methano-naphthalene (1.0 mmol, 304 mg). A magnetic stir bar was added, and the open vial was gently flushed with N2. Dioxane (2 mL) was added, followed by N,N′-dimethylethylenediamine (0.45 mmol, 48 μl). The vial was sealed and placed into a preheated screening block at 130° C. Conversion was complete after 24 hours. The yield (HPLC-analysis) of the compound of formula I was 70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524915B2
Source datasetuspto-grants-2013_09
ORD IDord-b89b478781c043a5bfaf4608bfeb2eda
Source noteuspto-grants-2013_09