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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522758Generated: October 27, 2026

N,N'-Dimethylethylenediamine → 6-chloro-7-fluoro-1-(1-propyl-1H-pyrazol-4-yl)-1H-indole

https://huagongshe.com/reaction/522758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Bromo-1-propyl-1H-pyrazoleHCID 21859707—
Reactant6-chloro-7-fluoro-1H-indoleHCID 22612745—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product6-chloro-7-fluoro-1-(1-propyl-1H-pyrazol-4-yl)-1H-indoleHCID 11810420072.2%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a stirred solution of compound 2 (1.1 g, 6.48 mmol) in toluene (15 mL) under inert atmosphere were added N,N′-dimethyl ethylene diamine (229 mg, 2.60 mmol), potassium phosphate (3.44 g, 16.27 mmol), 4-bromo-1-propyl-1H-pyrazole (Intermediate B; 1.21 g, 6.50 mmol), CuI (124 mg, 0.65 mmol) at RT, degassed under argon for 15 min; heated to 140° C. and stirred for 20 h in sealed tube. The reaction was monitored by TLC; after completion of the reaction, the reaction mixture was diluted with EtOAc (30 mL), filtered and the filtrate was concentrated under reduced pressure to obtain the crude. This was purified by silica gel column chromatography using 8-10% EtOAc/Hexanes to afford compound 3 (1.3 g, 72%) as brown liquid. 1H NMR (500 MHz, CDCl3): δ 7.64 (s, 1H), 7.60 (s, 1H), 7.31 (d, J=7.5 Hz, 1H), 7.12-7.07 (m, 2H), 6.60 (s, 1H), 4.13 (t, J=7.0 Hz, 2H), 1.99-1.91 (m, 2H), 0.97 (t, J=8.0 Hz, 3H); LC-MS (ESI): 93.5%; m/z 278.2 (M+H+); (column: X Select CSH C-18, 50×3.0 mm, 3.5 μm); RT 4.08 min; 5 mM NH4OAc: ACN; 0.8 mL/min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334261B2
Source datasetuspto-grants-2016_05
ORD IDord-c61f8296ebf540a0b53e0e6a4c592361
Source noteuspto-grants-2016_05