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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499202Generated: October 30, 2026

Water → HCID 11634218, compound

https://huagongshe.com/reaction/499202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylateHCID 22181157—
Reactant2,2,2-Trichloroethyl (3-tert-butyl-1-methyl-1H-pyrazol-5-yl)carbamateHCID 59420872—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
ProductHCID 11634218HCID 11634218—

Reaction Conditions

Temperature60 °C

Reaction Steps

Nitrogen gas is bubbled through a solution of (5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-carbamic acid 2,2,2-trichloro-ethyl ester (1.65 g, 5.01 mmol) and 4-(4-amino-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester (1.47 g, 5.02 mmol) in DMSO (20 mL) for 2 min. Next, N,N-diisopropylethylamine (2 mL, 11.48 mmol) is added. The reaction mixture is stirred at 60° C. for 6 hours. Then, the reaction mixture is distributed between water (150 mL) and dichloromethane (100 mL). The aqueous layer is isolated and extracted with dichloromethane (2×100 mL). The combined organic phases are washed with water (100 mL) and aqueous sodium chloride (100 mL), and dried over anhydrous sodium sulfate. After removal of solvent, the crude product is purified on a silica gel chromatography with ethyl acetate-hexanes (25%) to give a white solid (2.28 g, 97%, ES−(m/z) 470.1 [M−H]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767674B2
Source datasetuspto-grants-2010_08
ORD IDord-3901c7dee0d34ea6801aa2ce7f54ff47
Source noteuspto-grants-2010_08