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 Tebipenem

Tebipenem synthesis

4synthesis methods
161715-20-4 Synthesis
4-Nitrobenzyl(1R,5S,6S)-6-[(R)-1-hydroxyethyl]-1-Methyl-2-[1-(1,3-thiazolin-2-yl)azetidin -3-yl]thio-1-carbapen-2-eM-3-carboxylate

161715-20-4
37 suppliers
inquiry

Tebipenem

161715-21-5
79 suppliers
inquiry

-

Yield: 94.5%

Reaction Conditions:

with hydrogen in water;butan-1-ol at 20; under 15001.5 Torr; for 4 h;Solvent;Pressure;Reagent/catalyst;

Steps:

1
The compound (II) (R is p-nitrobenzyl) (15.0 g, 29.Ommo 1) was added 200 mL of n-butanol, 200 mL of water, stirred to dissolve, and 8.00 g of Raney Ni was added and hydrogenated at 20 ° C under 2.0 MPa hydrogen pressure for 4 h. The filter cake was washed with 15 mL of water The filtrate was adjusted to pH 6.5 with 4-dimethylaminopyridine and then washed with 150 mL of ethyl acetate. After cooling to 0 ° C, 700 mL of acetone was added dropwise, stirred for 10 min and then 700 mL of acetone was added dropwise, stirred for 1 h, To give telbemidine as a white solid 12.5 g, yield 94.5%, purity 99.6%.

References:

Shanghai Institute of Pharmaceutical Industry;Luo, ying;Liu, xiangkui;Shen, yuhui;Zhu, xueyan;Yuan, zhedong CN102757430, 2016, B Location in patent:Paragraph 0040; 0041

Tebipenem Related Search: