Process Development of a Diacyl Glycerolacyltransferase-1 Inhibitor
摘要:
A synthesis of a selective diacyl glycerolacyltransferase-1 (DGAT-1) inhibitor, 1, is described. The synthesis illustrates a diketone Favorskii reaction on 9 in place of the more common ketoester variant for generation of the dicarboxycyclopentane core, the development of an efficient classical resolution of a key cyclopentyl ketoacid intermediate 4, and an ambient temperature Suzuki-Miyaura coupling which avoids epimerization of the labile aryl ketone of 1.
Preparation and use of aryl alkyl acid derivatives for the treatment of obesity
申请人:Bayer Pharmaceuticals Corporation
公开号:US20040224997A1
公开(公告)日:2004-11-11
This invention relates to certain aryl alkyl acid compounds, compositions, and methods for treating or preventing obesity and related diseases.
这项发明涉及某些芳基烷基酸化合物、组合物以及治疗或预防肥胖和相关疾病的方法。
Inhibitors of diacylglycerol O-acyltransferase type 1 enzyme
申请人:Kym R. Philip
公开号:US20080015227A1
公开(公告)日:2008-01-17
The present invention relates to compounds of formula (I).
wherein R
1
, R
2
, R
3
, R
4
, R
5
, R
6
, m, n, p and q are defined herein Pharmaceutical compositions and methods for treating DGAT-1 related diseases or conditions are also disclosed.
Provided herein are compounds of the formula (I):
as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity, type II diabetes mellitus and metabolic syndrome.