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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446769Generated: October 25, 2026

2-(4-tert-Butylphenyl)cyclopropanecarbohydrazide → 2-(4-tert-butylphenyl)-N-[(E)-1-isoquinolin-5-ylethylideneamino]cyclopropane-1-carboxamide

https://huagongshe.com/reaction/446769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-tert-Butylphenyl)cyclopropanecarbohydrazideHCID 589199—
Reactant1-(Isoquinolin-5-yl)ethan-1-oneHCID 20493469—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product2-(4-tert-butylphenyl)-N-[(E)-1-isoquinolin-5-ylethylideneamino]cyclopropane-1-carboxamideHCID 4618625745.2%

Reaction Steps

A solution of 2-(4-tert-butylphenyl)cyclopropanecarbohydrazide (200 mg, 0.86 mmol) and 1-(isoquinolin-5-yl)ethanone (147 mg, 0.86 mmol) in 1,2-dichloroethane (10 mL) was stirred at room temperature for 2 h. The reaction mixture was then diluted with water (5 mL) and the organic layer was separated, washed brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The crude material was purified via silica gel column chromatography to afford (E)-2-(4-tert-butylphenyl)-N′-(1-(isoquinolin-5-yl)ethylidene)cyclopropanecarbohydrazide (150 mg, 45%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481532B2
Source datasetuspto-grants-2013_07
ORD IDord-293c0aa1fa3140b89398af1687bb6c1c
Source noteuspto-grants-2013_07