HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459649Generated: October 29, 2026
Trityl chloride → HCID 86597904, compound
https://huagongshe.com/reaction/459649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86597903 | HCID 86597903 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86597904 | HCID 86597904 | — |
Reaction Steps
To a solution of the crude product of di-tert-butyl (1S)-{1-[(5-amino-1-methyl-1H-pyrazol-4-yl)carbamoyl]pentamethylene}biscarbamate and triethylamine (0.91 g) in chloroform (30 ml) was added triphenylmethyl chloride (2.51 g), and the mixture was stirred at room temperature for 6 hours. The reaction mixture was washed successively with 0.10% aqueous citric acid solution, brine and saturated aqueous sodium hydrogencarbonate 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 3% methanol/chloroform to give di-tert-butyl (1S)-(1-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]carbamoyl}pentamethylene)biscarbamate (4.23 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192943B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-f223c81a918f41188bc064a712f0719f |
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| Source note | uspto-grants-2007_03 |
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