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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267535Generated: November 2, 2026

Diisopropylamine → HCID 11533779, compound

https://huagongshe.com/reaction/2267535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantPotassium CarbonateHCID 11430—
ReactantSulfamideHCID 82267—
Reactant3-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indole-7-carboxamideHCID 59003280—
ProductHCID 11533779HCID 1153377913%

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 N-(1-methylethyl)-2-propanamine (0.22 mL, 1.55 mmol) were allowed to react in the presence of K2CO3 (172.5 mg, 1.28 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% triflucaroacetic acid) to give the title compound (20.5 mg, 13%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858796B2
Source datasetuspto-grants-2010_12
ORD IDord-639c190e9718487e9936e7a11e60a875
Source noteuspto-grants-2010_12