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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301765Generated: October 30, 2026

Diisopropylethylamine → 1-(SR)-((t-Butoxycarbonyl)amino)-3-(SR)-((4-(N-(4-nitrobenzyloxycarbonyl)-N-(allyl)amino)piperidin-1-yl)methyl)-4-(SR)-phenylcyclopentane

https://huagongshe.com/reaction/2301765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(SR)-((t-butoxycarbonyl)amino)-3-(SR)-(formyl)-4-(SR)-phenylcyclopentaneHCID 18187642—
Reactant4-(N-(4-nitrobenzyloxycarbonyl)(N-allyl)amino)piperidine hydrochlorideHCID 18187675—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product1-(SR)-((t-Butoxycarbonyl)amino)-3-(SR)-((4-(N-(4-nitrobenzyloxycarbonyl)-N-(allyl)amino)piperidin-1-yl)methyl)-4-(SR)-phenylcyclopentaneHCID 18187603101.2%

Reaction Steps

To a solution of 1-((SR)-((t-butoxycarbonyl)amino)-3-(SR)-(formyl)-4-(SR)-phenylcyclopentane (from Step G, derived from Higher Rf isomer in Step E) (30 mg, 0.11 mmol) in 1,2-dichloroethane (3 mL) was added 4-(N-(4-nitrobenzyloxycarbonyl)(N-allyl)amino)piperidine hydrochloride (45 mg, 0.126 mmol) and DIPEA (0.022 mL, 0.126 mmol). After 15 min, sodium triacetoxyborohydride (45 mg, 0.22 mmol) was added and the reaction was stirred at RT for 6 h. The reaction was diluted with methylene chloride, quenched with aq. sodium carbonate and extracted 3 times with methylene chloride. The organic layers were each washed with brine, dried over sodium sulfate, combined and concentrated in vacuo. The residue was purified by Prep TLC eluting with 5% methanol in methylene chloride to give the title product (66 mg) as the free amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500844B1
Source datasetuspto-grants-2002_12
ORD IDord-342bc66a2a1b4404b06a114fc2f7ff2f
Source noteuspto-grants-2002_12