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 Ciprofloxacin
85721-33-1

Ciprofloxacin synthesis

11synthesis methods
Ciprofloxacin, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolincarboxylic acid (33.2.19), is synthesized in a completely analogous scheme, except that instead of using ethyl iodide in the alkylation stage, cyclopropyl bromide is used.
-

Yield:85721-33-1 960 mg

Reaction Conditions:

in (methylsulfinyl)methane;Heating;

Steps:

2 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-l-yl)-l,4-dihydroquinoIine-3-carboxylic acid (1)

To a solution of 7 (3.77 mmoles) in DMSO (30 mL) in a round bottom flask was added the piperazine ( 15 mmoles) and the mixture was heated to 90 °C. The reaction was monitored by HPLC. Upon complete consumption of the starting material, the reaction mixture was cooled to room temperature. 4 N HCl was added to the mixture to adjust the pH to 7. Ciprofloxacin (1) was allowed to gradually precipitate in a 4 °C fridge. The solid was filtered, washed three times with water and three times with acetone and dried, affording 960 mg yellow solid.

References:

WO2018/231747,2018,A2 Location in patent:Page/Page column 19; 33; 36-37

Ciprofloxacin Related Search: