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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459607Generated: October 25, 2026

Trityl chloride → Phenyl [1-methyl-5-(tritylamino)pyrazol-4-yl]carbamate

https://huagongshe.com/reaction/459607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantHeptaneHCID 8900—
Reactant5-Amino-1-methyl-4-phenoxycarbonylaminopyrazoleHCID 21904460—
SolventTetrahydrofuranHCID 8028—
ProductPhenyl [1-methyl-5-(tritylamino)pyrazol-4-yl]carbamateHCID 2190456780.7%

Reaction Steps

To a suspension of 5-amino-1-methyl-4-phenoxycarbonylaminopyrazole (153.8 g) in tetrahydrofuran (1 L) were added triethylamine (67 g) and triphenylmethyl chloride (185 g) at room temperature. The mixture was stirred for 6.5 hours. To the reaction mixture was added heptane (2.6 L) and the mixture was stirred for 1 hour. The precipitated solid was collected by filtration and washed with heptane-diisopropyl ether (1:1). The crude solid was suspended in water (3 L) and the suspension was stirred for 1 hour. The solid was collected by filtration and dried to give 1-methyl-4-phenoxycarbonylamino-5-triphenylmethylaminopyrazole (253.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192943B2
Source datasetuspto-grants-2007_03
ORD IDord-357565b0423249bda79dfe4b191372f4
Source noteuspto-grants-2007_03