成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List LX-4211
1018899-04-1

LX-4211 synthesis

6synthesis methods
Sotagliflozin is a dual SGLT-1/SGLT-2 inhibitor which is currently under development by Lexicon Pharmaceuticals (phase III). It follows a similar strategy to ertugliflozin, i.e. aryl addition on an acyclic precursor. The synthesis starts from L-xylose 53, and the aryl moiety (same aryl moiety as for dapagliflozin) is introduced on an amide derivative (morpholine amide 54) via Grignard addition. A subsequent transformation leads to the sotagliflozin (Scheme 10). The overall yield of the synthesis is around 30%.

Sotagliflozin synthesis
-

Yield:1018899-04-1 99.7%

Reaction Conditions:

with methanol;sodium methylate in toluene at 113; under 13501.4 Torr; for 0.00555556 h;Temperature;Pressure;

Steps:

1; 2; 3 Synthesis of sotagliflozin in toluene
Sotagliflozin was synthetized in an intensified reactor at 113°C under a pressure of 8 bar.The reactor was fed with the solution of compound (A) in 10 Volumes of toluene with a flow of 1194.6 g/h and the methanolic solution of MeONa (0.6 equivalent of MeONa and 15 equivalents of MeOH) with a flow of 114.6 g/h, which were preheated at 113°C.The time of residence in the reactor was 20 seconds.The system was maintained at a pressure of 8 bar.Sotagliflozin was synthetized with a yield of 99.7%.Aqueous washing, dehydration, crystallization, filtration, washing, drying were performed according to example 2.An XRPD (X-ray diffraction) analysis confirmed that Form II of sotagliflozin was obtained.

References:

LEXICON PHARMACEUTICALS, INC. WO2021/19507, 2021, A1 Location in patent:Page/Page column 9-12

FullText

LX-4211 Related Search: