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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254227Generated: November 2, 2026

tert-butyl (S)-2-amino-3-cyclohexylpropylcarbamate → tert-butyl (2S)-3-cyclohexyl-2-(2-(3-((2-fluorophenyl)(3-methoxypropoxy)methyl)piperidin-1-yl)-3,4-dioxocyclobut-1-enylamino)propylcarbamate

https://huagongshe.com/reaction/1254227

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (S)-2-amino-3-cyclohexylpropylcarbamateHCID 59382910—
Reactant3-(3-((2-Fluorophenyl)(3-methoxypropoxy)methyl)piperidin-1-yl)-4-methoxycyclobut-3-ene-1,2-dioneHCID 59383074—
SolventAcetonitrileHCID 6342—
Producttert-butyl (2S)-3-cyclohexyl-2-(2-(3-((2-fluorophenyl)(3-methoxypropoxy)methyl)piperidin-1-yl)-3,4-dioxocyclobut-1-enylamino)propylcarbamateHCID 5754493040%

Reaction Steps

To the crude 3-(3-((2-fluorophenyl)(3-methoxypropoxy)methyl)piperidin-1-yl)-4-methoxycyclobut-3-ene-1,2-dione in MeCN there was added tert-butyl (S)-2-amino-3-cyclohexylpropylcarbamate (27.0 mg, 0.11 mmol), the resulting solution was stirred at rt for 10 min, filtered through HPLC filter, purified by HPLC to give tert-butyl (2S)-3-cyclohexyl-2-(2-(3-((2-fluorophenyl)(3-methoxypropoxy)methyl)piperidin-1-yl)-3,4-dioxocyclobut-1-enylamino)propylcarbamate (17.4 mg, 40%) as on oil. MS ESI +ve m/z 616 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455521B2
Source datasetuspto-grants-2013_06
ORD IDord-9db3bd531f34403d9659f835161440eb
Source noteuspto-grants-2013_06