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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923Generated: October 25, 2026

4-(Aminomethyl)piperidine → (R)-alpha-Amino-N-methyl-N-[(2'-nitro)[1,1'-biphenyl]-4-yl]-benzenebutanamide

https://huagongshe.com/reaction/1923

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminomethyl)piperidineHCID 23527—
Reactant(R)-alpha-[N-(9-Fluorenylmethoxycarbonyl)amino]-N-methyl-N-[(2'-nitro)[1,1'-biphenyl]-4-yl]-benzenebutanamideHCID 22883387—
SolventDichloromethaneHCID 6344—
Product(R)-alpha-Amino-N-methyl-N-[(2'-nitro)[1,1'-biphenyl]-4-yl]-benzenebutanamideHCID 22883384—

Reaction Steps

The FMOC amide from Step F (1.15 g; 1.88 mmol) was dissolved in methylene chloride (10 ml) and 4-(aminomethyl)piperidine (1 ml) added. The reaction mixture was stirred at room temperature. The reaction mixture was stirred for 15 minutes and then quenched by adding water. The methylene chloride phase was separated, dried over ahnydrous potassium carbonate powder, filtered and evaprated under reduced pressure to afford an orange-yellow oil. The oil was chromatographed on silica gel using an eluant of ethyl acetate and methanol (9:1 v/v). A pale yellow oil (517 mg; 70.6%) was isolated of the amine. FAB-MS:- calculated for C23H23N3 O3 389.2 found 389.9 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726319
Source datasetuspto-grants-1998_03
ORD IDord-4973b5510ea745408780d7b531a293b6
Source noteuspto-grants-1998_03