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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322706Generated: October 29, 2026

Tert-butoxycarbonylalanine → N-[N-(Pent-4-enoyl)-L-alaninyl]-phenylalanine Methyl Ester

https://huagongshe.com/reaction/322706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantL-Phenylalanine, methyl esterHCID 736234—
ReactantAlanylphenylalanine methyl esterHCID 12988705—
SolventDichloromethane methanolHCID 21226129—
ProductN-[N-(Pent-4-enoyl)-L-alaninyl]-phenylalanine Methyl EsterHCID 9880679—

Reaction Steps

Following General Procedure A and using N-(L-alaninyl)-L-phenylalanine methyl ester (prepared by coupling N-BOC-L-alanine (Sigma) and L-phenylalanine methyl ester (Sigma) using General Procedure A, followed by removal of the BOC-group using General Procedure Y) and pent-4-enoic acid (Aldrich), the title compound was prepared as a solid (mp=125.5-126.5° C.). The reaction was monitored by tlc (Rf=0.32 in 50% EtOAc/hexanes; 0.51 in 10% CH3OH/CH2Cl2) and the product was purified by flash chromatography using 10% CH3OH/CH2Cl2 as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211235B1
Source datasetuspto-grants-2001_04
ORD IDord-d33a30efb3ad43c08c8effc2bb3c6794
Source noteuspto-grants-2001_04