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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929339Generated: October 31, 2026

Cyclopropanecarboxylic acid → HCID 68513327, compound

https://huagongshe.com/reaction/1929339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboxylic acidHCID 15655—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178484287HCID 178484287—
ReactantHCID 178525664HCID 178525664—
SolventDimethylformamideHCID 6228—
ProductHCID 68513327HCID 6851332728.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

a solution of 270 mg of 1-[bis(dimethylamino)methylidene]-2,3-dihydro-1H-[1,2,3]triazolo[4,5-b]pyridin-1-ium-3-oxide hexafluorophosphate, 61 mg of cyclopropanecarboxylic acid and 176 mg of diisopropylethylamine in 40 cm3 of N,N-dimethylformamide is stirred for one hour at a temperature close to 20° C. Then 250 mg of 6-[(2,6-dichlorobenzyl)oxy]-1H-benzimidazol-2-aminium trifluoroacetate is added and the orange solution obtained is stirred for about twenty hours at about 20° C. After concentration under reduced pressure (0.2 kPa), the residue is taken up in 40 cm3 of water and the mixture obtained is extracted three times with 40 cm3 of ethyl acetate. The combined organic phases are washed three times with 40 cm3 of water, then dried over magnesium sulphate, filtered and concentrated under reduced pressure. After purification of the residue by flash chromatography on silica [eluent: dichloromethane/methanol (95/5 by volume)], we obtain 64 mg of N-{6-[(2,6-dichlorobenzyl)oxy]-1H-benzimidazol-2-yl}cyclopropanecarboxamide in the form of a white powder, which has the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188078B2
Source datasetuspto-grants-2012_05
ORD IDord-0b7b7ba935d4475e885f4c8a0beefbd1
Source noteuspto-grants-2012_05