Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465432Generated: October 31, 2026

4'-Bromoacetanilide → Tert-butyl 2-({4-[(4-acetamidophenyl)ethynyl]phenyl}acetyl)hydrazinecarboxylate

https://huagongshe.com/reaction/1465432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-BromoacetanilideHCID 7683—
ReactantDiisopropylamineHCID 7912—
ReactantTriphenylphosphineHCID 11776—
ReactantTert-butyl 2-[(4-ethynylphenyl)acetyl]hydrazinecarboxylateHCID 86651837—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 2-({4-[(4-acetamidophenyl)ethynyl]phenyl}acetyl)hydrazinecarboxylateHCID 6703002420.2%

Reaction Steps

Palladium (II) acetate (2.5 mg, 0.011 mmol) and triphenylphosphine (11 mg, 0.044 mmol) were added to diisopropylamine (4 ml), and the mixture was stirred at room temperature for 20 mins. N-(4-Bromophenyl)acetamide (78 mg, 0.365 mmol) and tert-butyl 2-[(4-ethynylphenyl)acetyl]hydrazinecarboxylate (100 mg, 0.365 mmol) were added, and the mixture was stirred at 70° C. for 2 hrs. Anhydrous acetonitrile (2 ml) was added, and the mixture was further stirred at 70° C. for 1 hr. The reaction mixture was cooled and concentrated. The residue was purified by silica gel column chromatography (dichloromethane:methanol=97:3) to give tert-butyl 2-({4-[(4-acetamidophenyl)ethynyl]phenyl}acetyl)hydrazinecarboxylate (30 mg, yield 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-561813911a7543208f638708e7d94705
Source noteuspto-grants-2015_04