Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-butyl N-(2-hydroxyethyl)carbamate | HCID 2733206 | — |
| Reactant | 1H-Pyrazole, 4,5-diamine-1-methyl-, sulfate (1:1) | HCID 21904571 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 21904528 | HCID 21904528 | 29.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129232B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-4f52cf45ab19466eb71d41d41521af00 |
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| Source note | uspto-grants-2006_10 |
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