Incoterm: | CIF |
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Min. Order: | 1 Kilogram |
Delivery Time: | 7 Days |
Basic Info
Model No.: 123855-55-0
Additional Info
Packaging: 25KGS/DRUM
Productivity: 100T/Y
Brand: VOLSENCHEM
Place of Origin: CHINA
Product Description
P-Nitrophenyl 2-(furfuryl sulfinyl)acetate acid is side chain of Lafutidine Side chain CAS number 123855-55-0, the appearance is light brown crystalline powder, usually Process condensation reaction between the said chain intermediate and lafutidine N-1 to get lafutidine. The specific experimental procedure is as follows: Take 13.2gram Lafutifine N-1 intermediate, add 70ml ethyl acetate, stirred to dissolve, then add 15.6gram 2- (2- furyl methylsulfinyl) acetic acid p-nitrophenol ester , the reaction material was stirred at room temperature for 3-4 hours, after completion of TLC detection, add 100ml water, with concentrated hydrochloric acid to adjust the PH to 4, filtered, layered, the aqueous phase was added 150ml dichloromethane, add potassium carbonate to adjust PH to 10 or so, stratified, the water layer add 80mL dichloromethane to extract. The organic phases were combined, washed 4 times with 30% potassium carbonate solution and washed 5 times with water. The organic phase was separated, dried over anhydrous sodium sulfate, filtered and concentrated to dryness. 100 mL of ethyl acetate was added and the precipitated crystals were stirred at room temperature. The crude product is recrystallized from anhydrous ethanol, decoloured with activated charcoal, filtered through hot water, crystallized by ice-water cooling, filtered and dried to obtain 13.5 g white solid lafutifine. The manufacturing process of P-Nitrophenyl 2-(furfuryl sulfinyl)acetate acid CAS123855-55-0 is not complicated, and it is not impossible to prepare it according to the method of patent. However, the patented method suits the situation of self-use of the product. If it is sold to abroad, it may be necessary to explore a more optimized method.
In a large number of synthetic lafutidine patent introduction, Lafutidine intermediates 3 CAS number 123855-55-0 is often synthesized as an active ester intermediate with the corresponding intermediate,take condensation reaction to synthesis lafutidine. The general procedure is as following: use (Z) -2 - ((4-bromobut-2-en-1-yl) oxy) -4- (piperidin-1-ylmethyl) pyridine as raw material to add phthalimide Potassium salt,subjected to a two-step reaction to give intermediate primary amine, primary amine and lafutidine intermediate 3 by condensation to give lafutidine. At present, most manufacturers use this method to synthesis, but this method has obvious shortcomings, the purity of primary amine is too low, and ultimately affect the purity of raw materials. There are few reports about the synthesis of lafutidine intermediate 3 CAS number 123855-55-0, which is only a simple role as an active ester in the amidation reaction, and there is no more in-depth introduction. Specific synthesis methods still need R & D persons to develop according to their own synthesis theory and experience.
Thera. Category:Antiulcerative
Cas No.:123855-55-0
Synonym:p-nitrophenyl 2-(furfurylsulfinyl)acetate;(FURAN-2-YL-METHANESULFINYL) ACETIC ACID 4-NITROPHENYL ESTER;4-NITROPHENYL 2-(FURAN-2-YL-METHYLSULFINYL)ACETATE;4-nitrophenyl 2-(furfurylsulfinyl)acetic acid;
Molecular Formula:C13H11NO6S
Molecular Weight:309.29
Pharmacopeia: In house Spec.
Specifications:Available on request
Packing:Export worthy packing
Material Safety Data Sheet:Available on request
Usage :Intermediates for Lafutifine
Competitive Advantage: Good quality and favorable price
Related intermediate of Lafutidine
1) 4-Nitrophenyl 2-(furfurylsulfinyl)acetic acid CAS 123855-55-0)
2) N-{4-[4-(Piperidinomethyl)pyridyl-2-oxy]-cis-2-butene}phthalimide maleic acid CAS 146447-26-9
3) 2-Chloroisonicotinic acid CAS 6313-54-8
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