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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879482Generated: October 29, 2026

Water → 5-bromo-1-methyl-3-(4-methylpiperazin-1-yl)-1H-indazole

https://huagongshe.com/reaction/879482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantNitrogen mustard hydrochlorideHCID 5935—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-1-methyl-1H-indazol-3-amineHCID 26369215—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-bromo-1-methyl-3-(4-methylpiperazin-1-yl)-1H-indazoleHCID 85843447—

Reaction Conditions

Temperature100 °C

Reaction Steps

A vessel was charged with 5-bromo-1-methyl-1H-indazol-3-amine (250 mg, 1.10 mmol), 2-chloro-N-(2-chloroethyl)-N-methylethanamine hydrochloride (230 mg, 1.21 mmol), H2O (250 μL), K2CO3 (500 mg, 3.63 mmol), and DMF (2.5 mL). The vessel was sealed and heated to 100° C. for 18 h. The reaction was poured into EtOAc and washed with 5% w/v aq LiCl (3×), dried (Na2SO4), filtered, and concentrated. The residue was treated with DCM and purification by flash column chromatography on silica gel (hexanes/ethyl acetate to remove side products; then DCM/MeOH eluent to elute product) provided 5-bromo-1-methyl-3-(4-methylpiperazin-1-yl)-1H-indazole. LCMS-ESI+: calc'd for C13H17BrN4: 309.1, 311.1 (M+H+); Found: 309.2, 311.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-38a56bff9d66423d94559736c6571690
Source noteuspto-grants-2015_03