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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079488Generated: October 30, 2026

Dimethylformamide → HCID 15382660, compound

https://huagongshe.com/reaction/1079488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3-Chloropropoxy)-3-methoxyacetophenoneHCID 7314264—
Reactant6-fluoro-3-piperazin-1-yl-1H-indazoleHCID 9815871—
SolventWaterHCID 962—
ProductHCID 15382660HCID 15382660106.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

A stirred mixture of 6-fluoro-3-(1-piperazinyl)-1H-indazole (2.3 g, 100 mmol), K2CO3 (1.5 g), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (2.8 g, 11 mmol), several crystals of KI and dimethylformamide (60 ml) was heated at 90° C. for 16 hours. The reaction was poured into H2O, and the aqueous suspension was extracted with ethyl acetate. The ethyl acetate was washed (H2O), dried (MgSO4) and concentrated to afford 5.0 g of a yellow oil. The oil was chromatographed on a Waters Prep 500 utilizing silica gel columns and eluting with methylene chloride/methanol (7%). Concentration of the desired fractions yielded 2.0 g (46%) of an off-white solid. This sample was combined with 1.0 g of a previous sample, and this was recrystallized from toluene to afford 2.6 g of 1-[4-[3-[4-(6-fluoro-1H-indazol-3-yl)-1-piperazinyl]-propoxy]-3-methoxyphenyllethanone as a white solid, m.p.=135°-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580875
Source datasetuspto-grants-1996_12
ORD IDord-df7b07a1160a45f983e98eefc841e2f1
Source noteuspto-grants-1996_12