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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979959Generated: October 29, 2026

N-(1-Carbobenzyloxy-5-phthalimidopentyl)-alpha-azaalanyl-(L)-proline-t-butyl ester → N-(1-Carboxy-5-phthalimidopentyl)-alpha-azaalanyl-(L)-proline-t-butyl ester

https://huagongshe.com/reaction/979959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-Carbobenzyloxy-5-phthalimidopentyl)-alpha-azaalanyl-(L)-proline-t-butyl esterHCID 18606049—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
ProductN-(1-Carboxy-5-phthalimidopentyl)-alpha-azaalanyl-(L)-proline-t-butyl esterHCID 1860606596.7%

Reaction Steps

A solution of azapeptide ester 24 (0.402 g; 0.679 mmol) in ethyl acetate (5 ml) and acetic acid (0.2 ml) was hydrogenated with 110 mg of 10% Pd C for 18 hours. Filtration of catalyst and removal of solvent gave azapeptide 25 as a white foam (0.330 g). TLC (silica gel; EPAW 20:5:1:1) Rf=0.7. MS m/e 574 (M+, monotrimethylsilyl). NMR (CDCl3): δ1.42 (9H.s); 1.5-2.1 (10H,m); 3.00 (3H,s); 3.4-3.8 (5H,m); 4.3-4.6 (1H,m); 7.6-7.8 (4H,m); 7.8-8.0 (1H, broad).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04634715
Source datasetuspto-grants-1987_01
ORD IDord-bbccc7cf8b4946ab938246fc04b88db1
Source noteuspto-grants-1987_01