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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178255Generated: October 26, 2026

Water → 4-(6-fluoro-3-oxo-1,3-dihydro-2H-pyrazolo[4,3-c]cinnolin-2-yl)-N-(1,2,2,6,6-pentamethylpiperidine-4-yl)benzamide

https://huagongshe.com/reaction/1178255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1,2,2,6,6-pentamethylpiperidineHCID 693792—
Reactant4-(6-fluoro-3-oxo-1,3-dihydro-2H-pyrazolo[4,3-c]cinnolin-2-yl)benzoyl chlorideHCID 58974858—
Solvent1-ButanolHCID 263—
SolventDimethylacetamideHCID 31374—
Product4-(6-fluoro-3-oxo-1,3-dihydro-2H-pyrazolo[4,3-c]cinnolin-2-yl)-N-(1,2,2,6,6-pentamethylpiperidine-4-yl)benzamideHCID 58974915—

Reaction Steps

4-(6-fluoro-3-oxo-1,3-dihydro-2H-pyrazolo[4,3-c]cinnolin-2-yl)benzoyl chloride (100 mg, 0.29 mmol) was dissolved in anhydrous DMA (2 ml). Diisopropylethylamine (75 mg, 101 μl, 0.58 mmol) was added followed by 4-amino-1,2,2,6,6-pentamethylpiperidine (49 mg, 0.29 mmol). The mixture was stirred overnight. Water (5 ml) and n-butanol (5 ml) were added. The phases were separated. The organic phase was washed with water (2×5 ml) and the solution was concentrated under vacuum. The title compound was isolated as a dark red solid (50 mg, 0.105 mmol, 36%). LCMS: m/z [M+H]+ 477.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276505B2
Source datasetuspto-grants-2007_10
ORD IDord-761687a7bdcd4513bd3c16825c234e20
Source noteuspto-grants-2007_10