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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821346Generated: October 31, 2026

1,2-Dichloroethane → (E)-2-[2-(1H-indazol-3-yl)vinyl]-N-(thiophen-2-ylmethyl)benzamide

https://huagongshe.com/reaction/1821346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
Reactant(2-Thienylmethyl)amineHCID 34005—
Reactant(E)-2-[2-(1H-indazol-3-yl)vinyl]benzoic acidHCID 57586985—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(E)-2-[2-(1H-indazol-3-yl)vinyl]-N-(thiophen-2-ylmethyl)benzamideHCID 6899797223.5%

Reaction Steps

A solution of (E)-2-[2-(1H-indazol-3-yl)vinyl]benzoic acid (35 mg, 0.13 mmol) obtained in Step 1 of Example 47 in THF (1.0 mL) was sequentially added with 4-methylmorpholine (29 μL, 0.27 mmol), 2-(aminomethyl)thiophene (23 mg, 0.28 mmol) and EDC (36 mg, 0.19 mmol) and stirred at room temperature for 1.0 hour. The reaction mixture was added with water and ethyl acetate to separate the mixture into organic layer and aqueous layer and the organic layer was concentrated under reduced pressure. The residue was purified by silica gel chromatography (chloroform/methanol=100/0 to 90/10) and the obtained compound was crystallized from a mixed solvent of hexane/ethyl acetate (9/1, 1.0 mL) to obtain Compound 141 (11 mg, 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605272B2
Source datasetuspto-grants-2009_10
ORD IDord-5aa7cf654ae34db2b15be1516d708962
Source noteuspto-grants-2009_10