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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732518Generated: November 1, 2026

Ninhydrin → Benzyloxycarbonyl-L-valyl-L-leucyl-L-threonine methyl ester

https://huagongshe.com/reaction/1732518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNinhydrinHCID 10236—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantZ-Val-ONpHCID 112124—
ReactantBenzyloxycarbonyl-L-leucyl-L-threonine methyl esterHCID 54439782—
CatalystPalladiumHCID 23938—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductBenzyloxycarbonyl-L-valyl-L-leucyl-L-threonine methyl esterHCID 53923485—

Reaction Steps

Benzyloxycarbonyl-L-leucyl-L-threonine methyl ester (I, 3.8 g, 10 mmole) was dissolved in a mixture of 95% EtOH (50 ml) and 1 N HCl (10 ml) and hydrogenated in the presence of a 10% Pd on charcoal catalyst (0.8 g). After removal of the catalyst and the solvent the residue was dissolved in DMF (35 ml), treated with DIEA (1.6 ml, 10 mmole), benzyloxycarbonyl-L-valine p-nitrophenyl ester (4.3 g, 12 mmole) and HOBt (1.5 g, 10 mmole). After a negative spot test with ninhydrin indicated the completion of the reaction, the solvent was removed in vacuo and the residue triturated with CHCl3 (40 ml). The resulting solid was washed with CHCl3 (20 ml) and dried: 4.5 g (94%, mp 217°-8° C.,) unchanged after extraction with solvents, [α]D24 -11.7° (c 1.5, DMF); RfC 0.75; Thr 1.08; Val 0.98; Leu 1.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237046
Source datasetuspto-grants-1980_12
ORD IDord-065fcdcd96ec4e4f8d0f437e82a1a642
Source noteuspto-grants-1980_12