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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247820Generated: October 27, 2026

Diisopropylethylamine → tert-butyl 3-[(([1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino}carbonyl)amino]-1-azetidinecarboxylate

https://huagongshe.com/reaction/1247820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butyl 3-aminoazetidine-1-carboxylateHCID 1516507—
ReactantPhenyl [1-methyl-5-(tritylamino)pyrazol-4-yl]carbamateHCID 21904567—
SolventDichloromethaneHCID 6344—
Producttert-butyl 3-[(([1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino}carbonyl)amino]-1-azetidinecarboxylateHCID 2190451659.9%

Reaction Steps

To a suspension of phenyl [1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]carbamate (2.18 g) and tert-butyl 3-amino-1-azetidinecarboxylate (793 mg) in methylene chloride (20 ml) was added N-ethyldiisopropylamine (1.07 ml), and the mixture was stirred under reflux for 40 hours. To the reaction mixture was added methylene chloride, and the solution was washed successively with 10% aqueous citric acid solution, 10% aqueous sodium hydroxide solution and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with 10% methanol/methylene chloride to give tert-butyl 3-[({[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino}carbonyl)amino]-1-azetidinecarboxylate (1.52 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129232B2
Source datasetuspto-grants-2006_10
ORD IDord-47a2ade4df4c4939a1e105381e9fef14
Source noteuspto-grants-2006_10