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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503068Generated: October 31, 2026

Diisopropylethylamine → HCID 86722591, compound

https://huagongshe.com/reaction/1503068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3,3,3-Trifluoropropionic acidHCID 2777972—
ReactantHCID 86722592HCID 86722592—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductHCID 86722591HCID 8672259125%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred solution of (E)-2-bromo-N-methyl-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-enyl)benzohydrazide (200 mg, 0.46 mmol) in DCE (15 mL), was added 3,3,3-trifluoropropanoic acid (59 mg, 0.38 mmol), DMAP (46 mg, 0.42 mmol), EDC.HCl (65 mg, 0.42 mmol) and DIPEA (0.2 mL, 1.16 mmol). The reaction mixture was stirred at 25° C. for 12 h, then diluted with water and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. Purification by flash column chromatography (SiO2, 100-200 mesh; eluting with 30% hexane:EtOAc) afforded the title compound as a yellow solid (50 mg, 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211281B2
Source datasetuspto-grants-2015_12
ORD IDord-180a71d0873740e3bbd827e24862082a
Source noteuspto-grants-2015_12