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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888284Generated: November 2, 2026

Piperazine → HCID 178513526, compound

https://huagongshe.com/reaction/1888284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178513524HCID 178513524—
SolventAcetonitrileHCID 6342—
ProductHCID 178513526HCID 17851352649.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indazole-7-carboxamide (Intermediate 22) (20 mg, 0.0435 mmol) in acetonitrile (1 mL) was added K2CO3 (27 mg, 0.174 mmol), piperazine (18.9 mg, 0.219 mmol) and sodium iodide (0.8 mg, 0.00435 mmol). The reaction mixture was heated to 60° C. for 14 hrs. The solution was filtered and concentrated. The residue was purified by using a Gilson semi-preparative HPLC system with a YMC ODS-A (C-18) column 50 mm by 20 mm ID, eluting with 10% B to 80% B in 10 min, hold for 0.1 min where A=H2O (0.1% trifluoroacetic acid) and B=CH3CN (0.1% trifluoroacetic acid) pumped at 25 mL/min to afford the title compound (11.0 mg, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501780B2
Source datasetuspto-grants-2013_08
ORD IDord-7612d1bd6f444f8c939e3cafb198c292
Source noteuspto-grants-2013_08