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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256725Generated: October 26, 2026

Pyridoxal hydrochloride → Lhrh

https://huagongshe.com/reaction/256725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridoxal hydrochlorideHCID 6171—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantLhrhHCID 36523—
ReactantSodium AcetateHCID 517045—
CatalystCupric acetateHCID 8895—
SolventDimethylformamideHCID 6228—
ProductLhrhHCID 36523—
ProductErgoline-8-beta-carboxamide, 1-acetyl-9,10-didehydro-N-ethyl-6-methyl-HCID 3039342—

Reaction Steps

The synthesis of peptide Ac-D-Nal(2)-D-Phe(4 Cl)-D-Trp-Ser-Arg-D-Lys[(Cu++)(POL)2 (DL-A2 pr)]-Leu-Arg-Pro-D-Ala-NH2 was performed by reacting [Ac-D-Nal(2)1, D-Phe(4Cl)2, D-Trp3, Arg5,D-Lys(DL-A2 pr)6, D-Ala10 ]LHRH (Preparation VIII, 40 mg of a TFA salt) in DMF (0.2 ml) at pH 8 (adjusted with sodium hydroxide and sodium acetate) with pyridoxal hydrochloride (Aldrich, 4 mg) then, after standing at room temperature for 1 hour, with copper(II) acetate (3 mg in 0.05 ml water). The crude product was purified by HPLC under conditions given in Example XI (system iv) to yield [Ac-D-Nal(2)1,D-Phe(4Cl)2,D-Trp3,Arg5,D-Lys[(Cu++)(POL)2 (DL-A2 pr)]6,D-Ala10 ]LHRH (40 mg) with HPLC retention time of 6.3 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258492
Source datasetuspto-grants-1993_11
ORD IDord-339a528b6d524f81878ab9d910e2e5d8
Source noteuspto-grants-1993_11