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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459636Generated: October 27, 2026

1-benzyl 4-tert-butyl ((1S)-1-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]carbamoyl}tetramethylene)biscarbamate → tert-butyl (4S)-4-amino-5-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino)-5-oxopentylcarbamate

https://huagongshe.com/reaction/459636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-benzyl 4-tert-butyl ((1S)-1-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]carbamoyl}tetramethylene)biscarbamateHCID 86597889—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-butyl (4S)-4-amino-5-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino)-5-oxopentylcarbamateHCID 8659789042.5%

Reaction Steps

A solution of 1-benzyl 4-tert-butyl ((1S)-1-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]carbamoyl}tetramethylene)biscarbamate (6.4 g) in methanol (100 ml) was treated with 10% palladium on carbon (1.0 g) under a hydrogen atmosphere at room temperature for 6 days. After the catalyst was filtered off, the filtrate was concentrated in vacuo. The residue was triturated with ether and dried in vacuo to give tert-butyl (4S)-4-amino-5-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino}-5-oxopentylcarbamate (2.2 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192943B2
Source datasetuspto-grants-2007_03
ORD IDord-e2b0bdf1b4624b66b63133c31cbfd802
Source noteuspto-grants-2007_03