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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267536Generated: November 3, 2026

Sodium Iodide → HCID 59003343, compound

https://huagongshe.com/reaction/2267536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantSulfamideHCID 82267—
Reactant2,5-Dimethylpyrrolidine, (2R,5R)-HCID 641767—
Reactant3-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indole-7-carboxamideHCID 59003280—
ProductHCID 59003343HCID 5900334337%

Reaction Steps

Following the general procedure for aminosulfonamide formation outlined in example 2, 3-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indole-7-carboxamide (100 mg, 0.313 mmol) and (2R,5R)-2,5-dimethylpyrrolidine (449 mg, 1.56 mmol) were allowed to react in the presence of K2CO3 (886 mg, 0.63 mmol) and NaI (251 mg, 1.56 mmol). The resulting residue was purified by reverse phase HPLC eluting with 10% B to 80% B, where A=H2O (0.1% trifluoroacetic acid) and B=CH3CN (0.1% trifluoroacetic acid) to give the title compound (60 mg, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858796B2
Source datasetuspto-grants-2010_12
ORD IDord-6b3fb93cfa2e4a1b8bbc1107e4805fd7
Source noteuspto-grants-2010_12