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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247848Generated: October 31, 2026

Water → tert-butyl 4-({[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino)carbonyl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/1247848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantPhenyl [1-methyl-5-(tritylamino)pyrazol-4-yl]carbamateHCID 21904567—
SolventDimethylformamideHCID 6228—
Producttert-butyl 4-({[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino)carbonyl)-1-piperazinecarboxylateHCID 2190451185.6%

Reaction Steps

To a suspension of phenyl [1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]carbamate (4.6 g) in N,N-dimethylformamide (32 ml) were added triethylamine (1.08 g) and tertbutyl 1-piperazinecarboxylate (1.99 g). The reaction mixture was stirred for 3 hours and poured into water. The mixture was extracted with ethyl acetate, and the organic layer was concentrated in vacuo. The residue was purified by column chromatography on silica gel (ethyl acetate→ethyl acetate:ethanol=20:1) to give tert-butyl 4-({[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino}carbonyl)-1-piperazinecarboxylate (4.7 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129232B2
Source datasetuspto-grants-2006_10
ORD IDord-47a6894f0d294bd9a3db2ea86671a279
Source noteuspto-grants-2006_10