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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807714Generated: October 25, 2026

4-Nitrophenyl chloroformate → 1-(4-(4-(4-(1,1,1,3,3,3-Hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazine-1-carbonyl)phenyl)-3-(2-hydroxy-2-methylpropyl)urea

https://huagongshe.com/reaction/1807714

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant2-Propanol, 1-amino-2-methyl-HCID 95102—
Reactant(4-Aminophenyl)(4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazin-1-yl)methanoneHCID 86638547—
SolventDichloromethaneHCID 6344—
Product1-(4-(4-(4-(1,1,1,3,3,3-Hexafluoro-2-hydroxypropan-2-yl)benzyl)piperazine-1-carbonyl)phenyl)-3-(2-hydroxy-2-methylpropyl)ureaHCID 5917590924%

Reaction Steps

4-Nitrophenyl carbonochloridate (0.217 mmol, 43.7 mg) was added to a stirred solution of (4-aminophenyl)(4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)-piperazin-1-yl)methanone (0.217 mmol, 100 mg) in dichloromethane (1 mL). After 1 hour, 1-amino-2-methylpropan-2-ol (0.650 mmol, 58.0 mg) was added and stirring continued for 1 hour. The reaction mixture was purified by silica column chromatography (eluant dichloromethane/methanol 0% to 10%) to yield the title compound (30 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357679B2
Source datasetuspto-grants-2013_01
ORD IDord-a04dcdcba8114cc6a94bd72b18fb446d
Source noteuspto-grants-2013_01