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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358848Generated: October 31, 2026

Lithium Hydroxide → 4-(1-Piperidinesulfonylpiperidin-4-ylmethyl)-phenylamine

https://huagongshe.com/reaction/1358848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactant2,2,2-trifluoro-N-[4-(1-piperidinesulfonylpiperidin-4-ylmethyl)-phenyl]acetamideHCID 12094398—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-(1-Piperidinesulfonylpiperidin-4-ylmethyl)-phenylamineHCID 1209439980.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2,2,2-trifluoro-N-[4-(1-piperidinesulfonylpiperidin-4-ylmethyl)-phenyl]acetamide (0.48 g, 1.11 mmol) and lithium hydroxide (0.23 g, 5.54 mmol) in methanol (10 mL) and water (1 mL) was heated at 60° C. for about 2 hours. The reaction mixture was concentrated in vacuo, diluted with water, and extracted with dichloromethane. The organic extracts were washed with water and brine, and dried (Na2SO4). The residue was crystallized from ethyl acetate/hexanes, to give 4-(1-piperidinesulfonylpiperidin-4-ylmethyl)-phenylamine (0.30 g) as a white solid, m.p. 144-145° C.; Analysis for C17H27N3O2S: Calc.: C, 60.50; H, 8.06; N, 12.45; Found: C, 60.76; H, 8.07; N, 12.56.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596876B2
Source datasetuspto-grants-2003_07
ORD IDord-45308b2d386a414c9557b18aa73dbdc1
Source noteuspto-grants-2003_07