Scalable Synthesis of Diazeniumdiolates: Application to the Preparation of MK-8150
摘要:
Synthetic diazeniumdiolate (DAZD)-based nitric oxide is utilized to modulate the nitric oxide (NO) concentration in cellular environments and to control physiological processes, yet chemists are still struggling to find efficient and scalable methodologies that will enable them to access sufficient quantities of the high-energy diazeniumdiolate intermediates for biological studies. Now, a general, scalable, safer, and high-yielding new methodology adaptable to the large-scale synthesis of DAZDs has been developed.
A compound having the structure
useful for treating hypertension, Pulmonary Arterial Hypertension (PAH), congestive heart failure, conditions resulting from excessive water retention, cardiovascular disease, diabetes, oxidative stress, endothelial dysfunction, cirrhosis, pre-eclampsia, osteoporosis or nephropathy.
Application of an Oscillatory Plug Flow Reactor to Enable Scalable and Fast Reactions in Water Using a Biomass‐Based Polymeric Additive**
作者:Susanne Hammer、Filippo Nanto、Paolo Canu、Sándor B. Ötvös、C. Oliver Kappe
DOI:10.1002/cssc.202301149
日期:2024.1.22
The strategic application of oscillatory plug flow reactors enabled fast reactions in water as reactionmedium in the presence of hydroxypropyl methylcellulose, a biomass-based polymeric additive. Due to the smart dimensioning-based reactor design strategy, reactions were scaled-up directly without the need for reoptimization.
[EN] FXR SMALL MOLECULE AGONIST AND PREPARATION METHOD THEREFOR AND USE THEREOF<br/>[FR] AGONISTE DE PETITE MOLÉCULE FXR ET SON PROCÉDÉ DE PRÉPARATION ET SON UTILISATION<br/>[ZH] FXR小分子激动剂及其制备方法和用途
HETEROCYCLIC DERIVATIVES CONTAINING PRIMARY AMINO GROUPS AND DIAZENIUMDIOLATES
申请人:Merck Sharp & Dohme Corp.
公开号:EP2683687B1
公开(公告)日:2017-04-19
FXR SMALL MOLECULE AGONIST AND PREPARATION METHOD THEREFOR AND USE THEREOF
申请人:Shanghai Institute of Materia Medica, Chinese Academy of Sciences
公开号:US20220213083A1
公开(公告)日:2022-07-07
An FXR small molecule agonist and a preparation method therefor and a use thereof, having a structure as shown in formula (I). The compound represented by formula (I) has FXR agonistic activity and is capable of preparing drugs for treatment of FXR-related diseases.