HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459647Generated: October 29, 2026
Trityl chloride → tert-butyl (5S)-5-([3-(tert-butoxycarbonylamino)propionyl]amino}-6-([1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino}-6-oxohexylcarbamate
https://huagongshe.com/reaction/459647
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86597899 | HCID 86597899 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | tert-butyl (5S)-5-([3-(tert-butoxycarbonylamino)propionyl]amino}-6-([1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino}-6-oxohexylcarbamate | HCID 86597900 | — |
Reaction Steps
To a solution of the crude product of tert-butyl (5S)-6-[(5-amino-1-methyl-1H-pyrazol-4-yl)amino]-5-{[3-(tert-butoxycarbonylamino)propionyl]amino}-6-oxohexylcarbamate and triethylamine (0.50 g) in chloroform (30 ml) was added triphenylmethyl chloride (1.37 g), and the mixture was stirred at room temperature for 16 hours. The reaction mixture was washed successively with 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 tert-butyl (5S)-5-{[3-(tert-butoxycarbonylamino)propionyl]amino}-6-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino}-6-oxohexylcarbamate (1.62 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-f4e4bc8cfc5a471898c6cd4b734f86aa |
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| Source note | uspto-grants-2007_03 |
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