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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296651Generated: November 2, 2026

N-[N-(tert-Butoxycarbonyl)-O-benzyl-L-seryl]-D-leucine methyl ester → HCID 54521511, compound

https://huagongshe.com/reaction/2296651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[N-(tert-Butoxycarbonyl)-O-benzyl-L-seryl]-D-leucine methyl esterHCID 54078518—
SolventHydrogen chloride-ethyl acetateHCID 21866389—
ProductHCID 54521511HCID 54521511141.3%

Reaction Steps

N-[N-(tert-Butoxycarbonyl)-O-benzyl-L-seryl]-D-leucine methyl ester (545 mg) was dissolved in 4N HCl-AcOEt (5 ml), and the solution was stirred at ambient temperature for 1.5 hours. The solvent was evaporated in vacuo. The resulting oil was dissolved in dry MEOH (5 ml). Benzaldehyde (205 mg) and sodium cyanoborohydride (NaBH3CN, 97 mg) were added to this solution, and the reaction mixture was stirred at ambient temperature for 3 hours. Benzaldehyde (60 mg) and NaBH3CN (30 mg) were added to the reaction mixture and the was stirred at ambient temperature for 1.5 hours. After evaporation of the solvent in vacuo, the residue was partitioned by dissolving same in AcOEt and saturated aqueous NaHCO3 solution. The organic layer was washed with saturated sodium chloride (NaCl) solution, dried over MgSO4, and conentrated in vacuo. The residue was purified by SiO2 column chromotography (eluent: CHCl3) to give 376 mg of N-(N,O-dibenzyl-L-seryl)-D-leucine methyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489324B2
Source datasetuspto-grants-2002_12
ORD IDord-3039a7a90bae4f7780f1b3e1199a0a4c
Source noteuspto-grants-2002_12