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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401085Generated: November 2, 2026

1-Benzoyl-2-isopropylhydrazine → HCID 71468733, compound

https://huagongshe.com/reaction/1401085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzoyl-2-isopropylhydrazineHCID 18869—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 86711430HCID 86711430—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 71468733HCID 71468733—

Reaction Steps

To solution containing (E)-3-(1-(3-methylbut-2-enyl)-1H-indol-3-yl)acrylic acid (160 mg, 0.62 mmol, 1.0 equivalent), N′-isopropylbenzohydrazide (167.5 mg, 0.94 mmol, 1.5 equivalent) and HATU (357.4 mg, 0.94 mmol, 1.5 equivalent) dissolved in DMF (5.0 ml), N,N-diisopropylethylamine (DIPEA)(0.16 ml, 0.94 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=1:1) and dried so that yellow solid form of (E)-N′-isopropyl-N′-(3-(1-(3-methylbut-2-enyl)-1H-indol-3-yl)acryloyl)benzohydrazide was obtained. (99.8 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906952B2
Source datasetuspto-grants-2014_12
ORD IDord-c1136174a47d42db99854526539de480
Source noteuspto-grants-2014_12