Isavuconazonium sulfate

Isavuconazonium sulfate C화학적 특성, 용도, 생산

개요

Isavuconazonium sulfate is a broad spectrum antifungal agent that was codeveloped by Basilea Pharmaceutica (a subsidiary of Hoffmann-La Roche acquired in 2000) and Astellas Pharma, which obtained its first approval by the United States Food and Drug Administration (FDA) for the treatment of invasive aspergillosis and invasive mucormycosis, available as both oral and intravenous formulations. Isavuconazonium sulfate is a water-soluble prodrug, which is rapidly hydrolyzed by esterases (mainly butylcholinesterase) in plasma into the active moiety isavuconazole (BAL-4815) and an inactive cleavage product (BAL-8728). Isavuconazole inhibits cytochrome P450 (CYP)- dependent enzyme lanosterol 14-ademethylase (CYP51) and thereby inhibits the synthesis of ergosterol, a key component of the fungal cell membrane.4 Isavuconazole displayed potent fungistatic or fungicidal activity in vitro against a broad range of clinically important yeasts and molds, namely Candida spp., Cryptococcus spp., Trichosporon spp., Geotrichum capitatum, Pichia spp., Rhodotorula spp., Saccharomyces cerevisiae, Aspergillus spp., and most species known to cause mucormycosis (Mucorales mucorales). This broad range of antifungal activity renders this drug more clinically appealing compared to other azoles with narrower indications. Furthermore, isavuconazole does not require a cyclodextrin vehicle due to its water solubility, and currently does not require therapeutic drug monitoring. Moreover, isavuconazole has displayed improved safety and tolerability compared to voriconazole.

Synthesis

The synthesis of active moiety isavuconazole 8 was started with commercial 1-(2,5-difluorophenyl)-2-(1H-l,2,4-triazol-lyl) ethanone (1). Triazole 1 was treated with n-BuLi followed by exposure to propionitrile (2) and acidic quench to give racemic alcohol 3 in 65% yield. Next, resolution of this racemic alcohol was facilitated through the use of camphor derivative 4 to provide alcohol 5 in 38% yield and 99% ee. Nitrile 5 was then treated with concentrated H2SO4 and H2S to furnish thioamide 6, and this was followed by a cyclization reaction involving 4-(2-chloroacetyl)- benzonitrile (7) which gave rise to isavuconazole 8 in 81% yield across the two-step sequence.
The preparation of water-soluble side chain 15 was initiated from commercially available 2-chloronicotinic acid (9), which was converted to the corresponding tert-butyl ester 11 via acid halide 10 in excellent yield for the two-step protocol. Subjection of pyridyl chloride 11 to methanolic methylamine furnished aminopyridine 12 in 92% yield, and this compound was subsequently reduced with lithium aluminum hydride to give aminoalcohol 13 in 76% yield. Next, Nacylation of 13 with 1-chloroethyl chloroformate (14) followed by treatment with N-Boc-sarcosine under esterification conditions delivered chloroethyl ester 15 in 73% yield. The union of the aminopyridyl side chain 15 with thiazoloalcohol 8 was facilitated by reacting the two compounds in the presence of KI in acetonitrile, and this alkylation was followed by removal of the Boc group with hydrochloric acid to give rise to isavuconazonium iodide hydrochloride (16) in 79% yield. Finally, isavuconazonium sulfate (I) was prepared from 16 using an anion exchange resin in 93% yield to finish the construction of the API.

Isavuconazonium sulfate 준비 용품 및 원자재

원자재

준비 용품

Isavuconazonium sulfate 공급 업체

공급자	전화	이메일	국가	제품 수	이점
Guangzhou Tengyue Chemical Co., Ltd.	+86-86-18148706580 +8618826483838	evan@tyvovo.com	China	153	58
Pharmacodia (Beijing) Co.,Ltd	+86-400-851-9921	sales@pharmacodia.com	China	2317	55
Shanghai Chaolan Chemical Technology Center	QQ:65489617 15618227136	info@SuperLan-chem.com	China	9943	58
Cato Research Chemicals Inc.	020-81960175-877 18933936954	tianwen.zhan@cato-chem.com	China	7735	58
Pushan Industry (Shaanxi) Co., Ltd.	029-81310890 13571859809	info@pushanshiye.com	China	10009	58
Nantong QuanYi Biotechnology Co., Ltd	0513-66337626 18051384581	sales@chemhifuture.com	China	4659	58
Cato Research Chemicals Inc.	13342851930	3008394369@qq.com	China	3354	58