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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301774Generated: October 28, 2026

4-Fluorobenzoyl chloride → 1-(R)-(N-(Methyl)-N-(4-fluorophenylcarbonyl)amino)-3-(S)-((4-(N-(4-nitrobenzyloxycarbonyl)-N-(allyl)amino)piperidin-1-yl)methyl)-4-(S)-phenylcyclopentane

https://huagongshe.com/reaction/2301774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
Reactant1-(R)-(N-(methyl)-N-(t-butoxycarbonyl)amino)-3-(S)-((4-(N-(4-nitrobenzyloxycarbonyl)-N-(allyl)amino)piperidin-1-yl)methyl)-4-(S)-phenylcyclopentaneHCID 18345089—
Product1-(R)-(N-(Methyl)-N-(4-fluorophenylcarbonyl)amino)-3-(S)-((4-(N-(4-nitrobenzyloxycarbonyl)-N-(allyl)amino)piperidin-1-yl)methyl)-4-(S)-phenylcyclopentaneHCID 18345079—

Reaction Steps

Using essentially the same procedure as in Example 16, Step A and B but substituting 1-(R)-(N-(methyl)-N-(t-butoxycarbonyl)amino)-3-(S)-((4-(N-(4-nitrobenzyloxycarbonyl)-N-(allyl)amino)piperidin-1-yl)methyl)-4-(S)-phenylcyclopentane from Example 29, Step H in Step A and 4-fluorobenzoyl chloride in Step B, the title compound was prepared.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500844B1
Source datasetuspto-grants-2002_12
ORD IDord-ba05aedaaa054b1e803ec707af0136a9
Source noteuspto-grants-2002_12