Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301773Generated: October 31, 2026

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

https://huagongshe.com/reaction/2301773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorobenzoyl chlorideHCID 74376—
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-(3-fluorophenylcarbonyl)amino)-3-(S)-((4-(N-(4-nitrobenzyloxycarbonyl)-N-(allyl)amino)piperidin-1-yl)methyl)-4-(S)-phenylcyclopentaneHCID 18345078—

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 3-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-1cc3e8adbc284590a919440ac140e581
Source noteuspto-grants-2002_12