Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101850Generated: November 2, 2026

Hydrazine → 2-[4-Chloro-5-cyano-2-(difluoromethyl)-1H-indol-1-yl]acetohydrazide

https://huagongshe.com/reaction/2101850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant[4-chloro-5-cyano-2-(difluoromethyl)-1H-indol-1-yl]acetic acidHCID 57800318—
SolventTetrahydrofuranHCID 8028—
Product2-[4-Chloro-5-cyano-2-(difluoromethyl)-1H-indol-1-yl]acetohydrazideHCID 5780013352%

Reaction Steps

To a solution of [4-chloro-5-cyano-2-(difluoromethyl)-1H-indol-1-yl]acetic acid (0.050 g, 0.175 mmol) in anhydrous THF (2 mL), under N2, was added CDl (0.030 g, 0.184 mmol). The mixture was stirred at rt for 4 h and additional CDl (0.030 g, 0.184 mmol) was added. After 45 min, additional CDl (0.079 g, 0.49 mmol) was added. After 5 min, hydrazine (0.112 g, 3.5 mmol) was added and the mixture was stirred at rt for 30 min. The mixture was partitioned between EtOAc and 0.2N NaOH. The organic phase was washed with 0.2N NaOH and sat'd brine. The combined aqueous phases were extracted with EtOAc (×2). The second EtOAc phases were washed with sat'd NaHCO3 solution and brine. The organic phases were combined, dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography (0-10% MeOH—CH2Cl2 gradient) to afford the title compound (0.027 g, 52% yield): MS (ES) m/z 299 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572820B2
Source datasetuspto-grants-2009_08
ORD IDord-926738f418dc417695f494721487e1a8
Source noteuspto-grants-2009_08