Difelikefalin NEW

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Min. Order1KG
Purity99%
Cas No1024828-77-0
Supply Ability500kg
Update time2025-10-22

Shandong Hanjiang Chemical Co., Ltd

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China

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Chemical Properties

Product Name	Difelikefalin
CAS No	1024828-77-0
EC-No
Min. Order	1KG
Purity	99%
Supply Ability	500kg
Release date	2025/10/22

Product Name:	Difelikefalin
Synonyms:	Difelikefalin (CR845);Difelikefalin(CR-845, FE-202845);CKD-943;CKD-943; CR 845; FE 202845; KORSUVA; MR13A9;DIFELIKEFALIN;CR845;CR 845;CR845;FE 202845;KORSUVA
CAS:	1024828-77-0
MF:	C36H53N7O6
MW:	679.85
EINECS:
Product Categories:
Mol File:	1024828-77-0.mol

Difelikefalin Chemical Properties

Boiling point	1005.5±65.0 °C(Predicted)
density	1.214±0.06 g/cm3(Predicted)
pka	2.05±0.20(Predicted)
form	Solid
color	White to off-white
InChIKey	FWMNVWWHGCHHJJ-SKKKGAJSSA-N
SMILES	N1(C(=O)[C@@H](CCCCN)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC2=CC=CC=C2)NC(=O)[C@@H](CC2=CC=CC=C2)N)CCC(N)(C(O)=O)CC1

Safety Information

MSDS Information

Difelikefalin Usage And Synthesis

Description	Difelikefalin, a novel drug discovered by Cara Therapeutics and developed by Vifor Pharma, was approved by the USFDA and the European Medicines Agency (EMA) in 2021 for the treatment of moderate to severe pruritus (pruritus). It is a highly selective κ-type opioid receptor agonist administered as an intravenous injection. difelikefalin restricts its action to the peripheral nervous system, which reduces central nervous system side effects such as sedation, anxiety and hallucinations. This peripheral restriction makes difelikefalin potentially advantageous in the treatment of pruritus, especially in patients who experience refractory pruritus due to renal failure or other conditions.
Uses	Difelikefalin is used in the formation of oral formulations of kappa opioid receptor agonists for the treatment of variety of kappa opioid receptor-?assocd. diseases and conditions such as pain, pruritus and inflammation.
Synthesis	Chromatography-free hydrochloride synthesis of Difelikefalin: Firstly, the piperidine amino acid 21.1 was coupled with the fully protected d-lysine analogue 21.2 under conventional EDCI/HOBt peptide coupling conditions to produce the fully protected dipeptide 21.3 in 97% yield. Conventional hydrogenation reduction was used to remove the N-terminal benzyloxycarbonyl protection to afford the amine 21.4 in 91% yield. Subsequent treatment of dipeptide 21.4 with protected d-leucine (21.5) and the same peptide coupling method followed by deprotection of the benzyl protecting group afforded tripeptide 21.6 in yields of 99% and 48%, respectively. Notably, the lower yield of tripeptide 21.6 may be due to crystallisation implemented during purification using cyclohexane and ethyl acetate rather than failure of the reaction to complete. Pure tripeptide 21.6 was then treated with protected d-phenylalanine and subjected to the same peptide coupling method followed by deprotection of the benzyl protecting group to give tetrapeptide 21.8 in 99% yield at each step. Treatment of tetrapeptide 21.8 with d-BocPhe under conventional peptide coupling conditions yielded a fully protected pentapeptide in 99% yield. The pentapeptide methyl ester 21.10 was precipitated in 99% yield by deprotection of the global Boc protecting group using 6N hydrochloric acid in isopropanol and addition of toluene to the reaction mixture. Next, the methyl ester 21.10 was treated under standard saponification conditions and the reaction was burst with 1N hydrochloric acid to obtain the pentapeptide 21.11 as a hydrochloride salt. although not disclosed, it is conceivable that the saponification reaction of 21.10 was burst with acetic acid to obtain its difelikefalin as a commercially available acetate salt (Compound No. 21).

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