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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247796Generated: October 31, 2026

Trityl chloride → HCID 21904528, compound

https://huagongshe.com/reaction/1247796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
Reactant1H-Pyrazole, 4,5-diamine-1-methyl-, sulfate (1:1)HCID 21904571—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 21904528HCID 2190452829.6%

Reaction Steps

To a suspension of 1,1′-carbonyldiimidazole (2.0 g) in dehydrated chloroform (30 ml) was added a solution of tert-butyl N-(2-hydroxyethyl)carbamate (1.92 g) in dehydrated chloroform (10 ml) under ice-cooling, and the mixture was stirred at room temperature for 1 hour. To the reaction mixture were added N-ethyldiisopropylamine (2.2 ml) and 4,5-diamino-1-methylpyrazole sulfuric acid salt (2.58 g), and the mixture was stirred at room temperature for 17.5 hours. To the reaction mixture were added trityl chloride (3.42 g) and triethylamine (1.25 g). The mixture was stirred at room temperature for 2 hours. The reaction mixture was washed with 10% aqueous citric acid solution, brine and saturated aqueous sodium hydrogen carbonate solution. 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 5% methanol/chloroform to give 4-{[2-(tert-butoxycarbonylamino)ethoxycarbonyl]amino}-5-(tritylamino)-1-methylpyrazole (1.91 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129232B2
Source datasetuspto-grants-2006_10
ORD IDord-4f52cf45ab19466eb71d41d41521af00
Source noteuspto-grants-2006_10