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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401083Generated: November 1, 2026

1-Benzoyl-2-isopropylhydrazine → HCID 71468731, compound

https://huagongshe.com/reaction/1401083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzoyl-2-isopropylhydrazineHCID 18869—
ReactantDiisopropylethylamineHCID 81531—
Reactant(E)-3-(1-methyl-1H-indol-3-yl)acrylic acidHCID 5965649—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 71468731HCID 71468731—

Reaction Steps

To solution containing (E)-3-(1-methyl-1H-indol-3-yl)acrylic acid (50 mg, 0.24 mmol, 1.0 equivalent), N′-isopropylbenzohydrazide (66.43 mg, 0.37 mmol, 1.5 equivalent) and HATU (141.72 mg, 0.37 mmol, 1.5 equivalent) dissolved in DMF (5.0 ml), N,N-diisopropylethylamine (DIPEA)(0.06 ml, 0.37 mmol, 1.5 equivalent) was slowly drop-wise added and stirred at room temperature for 24 hr. The reaction mixture was diluted with EtOAc, washed with water and brine, dried with anhydrous MgSO4, filtered, and concentrated under reduced pressure. The residue was separated through silica gel chromatography (n-hexane:EtOAc:methanol=9:3:1) and dried so that white solid form of (E)-N′-isopropyl-N′-(3-(1-methyl-1H-indol-3-yl)acryloyl)benzohydrazide was obtained.(82.62 mg, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906952B2
Source datasetuspto-grants-2014_12
ORD IDord-4a8a5bf46f7a4669bba82167b548ffed
Source noteuspto-grants-2014_12