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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750159Generated: October 28, 2026

1-(2-Methoxyphenyl)piperazine → 6-(3-(4-(2-methoxyphenyl)piperazin-1-yl)propoxy)-1H-indazole

https://huagongshe.com/reaction/1750159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantSodium IodideHCID 5238—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-(3-(4-(2,3-dichlorophenyl)piperidin-1-yl)propoxy)-1H-indazoleHCID 66633774—
SolventAcetonitrileHCID 6342—
Product6-(3-(4-(2-methoxyphenyl)piperazin-1-yl)propoxy)-1H-indazoleHCID 5659736260%

Reaction Steps

A mixture of intermediate 44 (42.2 mg, 0.17 mmol) and NaI (49.5 mg, 0.33 mmol) in CH3CN (3 mL) was heated to reflux for 30 min and then cooled to rt. To this mixture was added intermediate 65 (35.0 mg, 0.18 mmol), followed then by DIEA (0.063 mL, 0.36 mmol). The resulting mixture was heated to reflux and stirred for 4 h. Precipitated crystals were filtered off and the filtrate was evaporated under reduced pressure. The residue was extracted with EtOAc. The combined EtOAc layers were washed with brine, dried over anhydrous Na2SO4, concentrated in vacuo and purified by ISCO to give 6-(3-(4-(2-methoxyphenyl)piperazin-1-yl)propoxy)-1H-indazole (compound 50) (36.6 mg, 60%). HPLC: 99%, RT 3.907 min. MS (ESI) m/z 367.20 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156822B2
Source datasetuspto-grants-2015_10
ORD IDord-f5a039376e6f4efaab283a78da415533
Source noteuspto-grants-2015_10