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ROLAPITANT HYDROCHLORIDE

CAS No.
914462-92-3
Chemical Name:
ROLAPITANT HYDROCHLORIDE
Synonyms
Rolapitant HCl hydrate;ROLAPITANT HYDROCHLORIDE;RolapitantMonohydrochloride;Rolapitant Hydrochloride Hydrate;Rolapitant Hydrochloride Monohydrate;(5S,8S)-8-(((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)methyl)-8-phenyl-1,7-diazaspiro[4.5]decan-2-one hydrochloride hydrate;(5S,8S)-8-[[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]methyl]-8-phenyl-1,9-diazaspiro[4.5]decan-2-one,hydrate,hydrochloride;(5S,8S)-8-[[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]methyl]-8-phenyl-1,7-Diazaspiro[4.5]decan-2-one hydrochloride hydrate (1:1:1);1,7-Diazaspiro[4.5]decan-2-one, 8-[[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]methyl]-8-phenyl-, hydrochloride, hydrate (1:1:1), (5S,8S)-;1,7-Diazaspiro[4.5]decan-2-one, 8-[[(1R)-1-[3,5-bis(trifluoroMethyl)phenyl]ethoxy]Methyl]-8-phenyl-, Monohydrochloride, Monohydrate, (5S,8S)-
CBNumber:
CB82666994
Molecular Formula:
C25H29ClF6N2O3
Molecular Weight:
554.96
MDL Number:
MFCD23105917
MOL File:
914462-92-3.mol
Last updated:2023-08-17 13:06:49

ROLAPITANT HYDROCHLORIDE Properties

Melting point >149oC (dec.)
storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
color White
NCI Dictionary of Cancer Terms rolapitant hydrochloride
FDA UNII 57O5S1QSAQ
NCI Drug Dictionary rolapitant hydrochloride

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS07
Signal word  Warning
Hazard statements  H361-H302
Precautionary statements  P201-P202-P281-P308+P313-P405-P501-P264-P270-P301+P312-P330-P501

ROLAPITANT HYDROCHLORIDE price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC R424505 RolapitantHydrochlorideHydrate 914462-92-3 5mg $275 2021-12-16 Buy
Biosynth Carbosynth FR162254 Rolapitant hydrochloride monohydrate 914462-92-3 50mg $350 2021-12-16 Buy
AK Scientific 2857CW Rolapitanthydrochloride 914462-92-3 25mg $387 2021-12-16 Buy
Biosynth Carbosynth FR162254 Rolapitant hydrochloride monohydrate 914462-92-3 100mg $450 2021-12-16 Buy
American Custom Chemicals Corporation API0014111 ROLAPITANT 95.00% 914462-92-3 5MG $498.99 2021-12-16 Buy
Product number Packaging Price Buy
R424505 5mg $275 Buy
FR162254 50mg $350 Buy
2857CW 25mg $387 Buy
FR162254 100mg $450 Buy
API0014111 5MG $498.99 Buy

ROLAPITANT HYDROCHLORIDE Chemical Properties,Uses,Production

Description

Rolapitant hydrochloride hydrate, originally discovered by Schering-Plough and later developed by TESARO, Inc., was approved by the FDA in September 2015 for the prevention of delayed chemotherapy-induced nausea and vomiting (CINV) in combination with other antiemetic agents. Rolapitant is a highly selective NK-1 receptor antagonist, exhibiting >1000- fold selectivity for NK-1 over human NK-2 and NK-3 receptors in vitro. In contrast to other NK-1 inhibitors that play an essential role in delayed CINV therapy, rolapitant shows no inhibition of CYP3A4, eliminating the need for concern when coadministering with CYP34A substrates. Additionally, rolapitant is an orally active agent with a relatively long half-life (180 h), providing potential opportunities for single- and prechemotherapy-based treatments. In three large clinical trials involving patients receiving moderately emetogenic chemotherapy (MEC) and highly emetogenic chemotherapy (HEC), subjects using rolapitant as a cotherapy with granisetron and dexamethasone showed a significant improvement in complete response compared to those receiving treatments of granisetron and dexamethasone.

Uses

Rolapitant Hydrochloride Hydrate is a raw material for pharmaceutical formulations.

Definition

ChEBI: A hydrate that is the monohydrate form of rolapitant hydrochloride. Used for the prevention of delayed nausea and vomiting associated with initial and repeat courses of emetogenic cancer chemotherapy.

Synthesis

Rolapitant features a fascinating molecular architecture consisting of two tetrasubstituted stereogenic carbon centers situated at the 2- and 5-carbons within a central piperidine ring and a spirocyclic array residing at the 5-position and a phenyl ring and ethereal linkage branching from the 2-position. The overall synthetic strategy to secure rolapitant hydrochloride hydrate relies upon the union of two advanced chiral building blocks that contain functional groups capable of securing the central piperidine ring. These two key intermediates, pyroglutamate derivative 93 and allylic amine 94, each bear one of the essential stereocenters embedded within the structure of the active pharmaceutical ingredient.
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The first of these advanced intermediates, amidoaldehyde 93, is generated directly by base-mediated decomposition of pyroglutamic aminal 92. Subjection of 92 to triethylamine in EtOH/H2O at ambient temperatures led to generation of chiral allyl aldehyde 93, which was not isolated but condensed immediately with amine 94 in the presence of refluxing toluene to provide divinyl imine 95, which underwent immediate reduction using NaBH(OAc)3 in AcOH/toluene to furnish the free amine. The free amine was converted to the corresponding tosylate monohydrate salt and triturated, providing 96 as a white crystalline powder after subjection to TsOH?¤H2O in i-PrOH/H2O. Divinyl amine 96 could then be reacted with a solution of TsOH in toluene, distilled, and directly combined with a toluene solution of Hoveyda-Grubbs second-generation catalyst (HG-II) under heating conditions, leading to the desired ring-closing metathesis product 97 as the HCl salt (85% yield over two steps) after filtration, distillation, and workup with 12N HCl. Washing of a toluene solution of 97 with aqueous NaOH and subsequent treatment of the resulting organic solution with H2, wet Pd/C, and additional granular activated carbon (Nuchar Aquaguard) led to the fully reduced piperidine product in high yield (95%). Rolapitant hydrochloride hydrate XIII was accessed thereafter by precipitation from a solution of EtOH/i-PrOH/H2O/HCl, providing the product as a white solid (91% yield).

Synthesis_914462-92-3

ROLAPITANT HYDROCHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 70)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Mojin Biotechnology Co., Ltd
+8613288715578 sales@hbmojin.com China 12470 58
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32715 60
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282 alice@crovellbio.com China 8829 58
HubeiwidelychemicaltechnologyCo.,Ltd
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career henan chemical co
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AFINE CHEMICALS LIMITED
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InvivoChem
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Hefei TNJ Chemical Industry Co.,Ltd.
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Hebei Duling International Trade Co. LTD
+8617333973358 sales01@hbduling.cn China 15620 58
Nanjing Doge Biomedical Technology Co., Ltd
+86-25-58227606 +86-15305155328 sales@dogechemical.com China 4128 58

View Lastest Price from ROLAPITANT HYDROCHLORIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
ROLAPITANT HYDROCHLORIDE pictures 2023-08-18 ROLAPITANT HYDROCHLORIDE
914462-92-3
US $50.00 / KG 1KG 99% 20TONS Hebei Mojin Biotechnology Co., Ltd
ROLAPITANT HYDROCHLORIDE pictures 2021-09-23 ROLAPITANT HYDROCHLORIDE
914462-92-3
US $10.00 / KG 100KG 99% 100 mt Hebei Guanlang Biotechnology Co., Ltd.
ROLAPITANT HYDROCHLORIDE pictures 2020-01-13 ROLAPITANT HYDROCHLORIDE
914462-92-3
US $9.80 / KG 1KG ≥98% 20 tons Career Henan Chemical Co
Rolapitant Hydrochloride Hydrate RolapitantMonohydrochloride ROLAPITANT HYDROCHLORIDE 1,7-Diazaspiro[4.5]decan-2-one, 8-[[(1R)-1-[3,5-bis(trifluoroMethyl)phenyl]ethoxy]Methyl]-8-phenyl-, Monohydrochloride, Monohydrate, (5S,8S)- (5S,8S)-8-[[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]methyl]-8-phenyl-1,9-diazaspiro[4.5]decan-2-one,hydrate,hydrochloride Rolapitant Hydrochloride Monohydrate Rolapitant HCl hydrate 1,7-Diazaspiro[4.5]decan-2-one, 8-[[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]methyl]-8-phenyl-, hydrochloride, hydrate (1:1:1), (5S,8S)- (5S,8S)-8-[[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]methyl]-8-phenyl-1,7-Diazaspiro[4.5]decan-2-one hydrochloride hydrate (1:1:1) (5S,8S)-8-(((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)methyl)-8-phenyl-1,7-diazaspiro[4.5]decan-2-one hydrochloride hydrate 914462-92-3 C25H29ClF6N2O3 C25H29CIF6N2O3H2O