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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929342Generated: October 25, 2026

Cyclopropanecarboxylic acid → N-{6-[(2,6-dichlorobenzyl)oxy]-1,3-benzothiazol-2-yl}cyclopropanecarboxamide

https://huagongshe.com/reaction/1929342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboxylic acidHCID 15655—
Reactant6-[(2,6-Dichlorobenzyl)oxy]-1,3-benzothiazol-2-amineHCID 86646938—
SolventPyridineHCID 1049—
ProductN-{6-[(2,6-dichlorobenzyl)oxy]-1,3-benzothiazol-2-yl}cyclopropanecarboxamideHCID 8664693760.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

add 23 mg of cyclopropanecarboxylic acid to a solution of 70 mg of 6-[(2,6-dichlorobenzyl)oxy]-1,3-benzothiazol-2-amine in 1.5 cm3 of anhydrous pyridine. After stirring for one hour at around 20° C., the reaction mixture is concentrated to dryness under reduced pressure (0.2 kPa). The residue is taken up in 25 cm3 of water, then the mixture obtained is extracted three times with 20 cm3 of dichloromethane. The combined organic phases are washed twice with 20 cm3 of water, dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure. After purification of the residue by silica-column flash chromatography [eluent: dichloromethane/methanol (92/8 by volume)], we obtain 51 mg of N-{6-[(2,6-dichlorobenzyl)oxy]-1,3-benzothiazol-2-yl}cyclopropanecarboxamide in the form of a cream-coloured powder, which has the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188078B2
Source datasetuspto-grants-2012_05
ORD IDord-4c0d563e25064802accfe65eec2d6e49
Source noteuspto-grants-2012_05