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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045164Generated: October 25, 2026

Water → 3-Nitro-4-(1-(tetrahydro-2h-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamide

https://huagongshe.com/reaction/1045164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Chloro-3-nitrobenzenesulfonamideHCID 7324—
ReactantTriethylamineHCID 8471—
Reactant1-(Tetrahydro-2H-pyran-4-yl)piperidin-4-amineHCID 22562145—
Solvent1,4-DioxaneHCID 31275—
Product3-Nitro-4-(1-(tetrahydro-2h-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamideHCID 67126384—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of EXAMPLE 173B (22.12 g), water (43 mL), and triethylamine (43.6 mL) in 1,4-dioxane (300 mL) was stirred at room temperature until EXAMPLE 173B completely dissolved. The solution was then treated with 4-chloro-3-nitrobenzenesulfonamide, heated at 90° C. for 16 hours, cooled and concentrated. 10% methanol in dichloromethane was added, and the solution was stirred vigorously at room temperature until a fine suspension existed and the mixture was filtered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563735B2
Source datasetuspto-grants-2013_10
ORD IDord-267e319029ab40ce967dad0db044042d
Source noteuspto-grants-2013_10