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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846098Generated: November 2, 2026

Pyridine → N-[4-Chloro-3-cyclopropylaminocarbonyl-phenyl]-2-chloro-5-(5-chloro-thien-2-yl)carbonylaminomethyl-benzamide

https://huagongshe.com/reaction/1846098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant5-amino-2-chloro-N-cyclopropylbenzamideHCID 16775240—
ReactantHCID 58483424HCID 58483424—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductN-[4-Chloro-3-cyclopropylaminocarbonyl-phenyl]-2-chloro-5-(5-chloro-thien-2-yl)carbonylaminomethyl-benzamideHCID 52919212—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 2.0 mL of a 0.05 M solution of 5-amino-2-chloro-N-cyclopropyl-benzamide (0.10 mmol) in acetonitrile was added pyridine (20 μL, 0.25 mmol) and then 1.0 mL of a 0.05 M solution of 2-chloro-5-(5-chloro-thien-2-yl)carbonylaminomethyl-benzoyl chloride (0.10 mmol, prepared from 5-(aminomethyl)-2-chloro-benzoic acid in analogy to step 1c and 1d) in acetonitrile. The reaction mixture was stirred overnight at 60° C., diluted with 200 μL of distilled water and filtered over Alox B. The Alox B pad was washed three times with 2.0 mL 9:1 DMF/MeOH-solution and the combined filtrate was concentrated in vacuo. The residue was dissolved in 2.0 mL of DMF and purified via prep. HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951999B2
Source datasetuspto-grants-2015_02
ORD IDord-1cce408dd085412e860a90ac83551cb1
Source noteuspto-grants-2015_02