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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667362Generated: October 26, 2026

Potassium Carbonate → Cyclopentyl(S)-2-[(4-Aminobenzyl)-tert-butoxycarbonyl amino]-4-methylpentanoate

https://huagongshe.com/reaction/1667362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Nitrobenzyl bromideHCID 66011—
Reactant(S)-cyclopentyl 2-amino-4-methylpentanoateHCID 53718217—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductCyclopentyl(S)-2-[(4-Aminobenzyl)-tert-butoxycarbonyl amino]-4-methylpentanoateHCID 57658375156.2%

Reaction Steps

4-Nitrobenzyl bromide (11 g, 50 mmol) was dissolved in DMF (180 ml) and potassium carbonate (13.6 g, 99 mmol) added, followed by L-leucine cyclopentyl ester (Intermediate 8) (16 g, 43 mmol). The reaction was stirred for 18 h at RT. The residue was diluted with EtOAc (500 ml) and washed with water (3×100 ml), dried (Na2SO4) filtered and concentrated to dryness to give the crude product (15.8 g) which was used in the next step without further purification. LCMS purity 60%, m/z 335 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044211B2
Source datasetuspto-grants-2011_10
ORD IDord-e1e8bf3b6d9b4e6ea8f871bb5d406d7c
Source noteuspto-grants-2011_10