摘要:
The present invention provides a new process for the preparation of 2S,3S-N-isobutyl-N-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide hydrochloride, wherein this compound is prepared directly from the chloromethylalcohol. Importantly, the process of the present invention results in higher yields of 2S,3S-N-isobutyl-N-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide hydrochloride without sacrificing its purity. The processes of the present inventin can be used to prepare not only the 2S,3S-derivative, but also the 2R,3S-, 2S,2R- and the 2R,3R-derivatives.
摘要:
This invention discloses a process for synthesizing an amine functionalized monomer that comprises (1) reacting a secondary amine with a 2,3-dihalopropene to produce a vinyl halide containing secondary amine having a structural formula selected from the group consisting of wherein R and R′ can be the same or different and represent allyl, alkoxyl or alkyl groups containing from 1 to about 10 carbon atoms, and wherein X represents a halogen atom, and wherein m represents an integer from 4 to about 10, and wherein X represents a halogen atom; and (2) reacting the vinyl halide containing secondary amine with a vinyl magnesium halide to produce the monomer having a structural formula wherein R and R′ can be the same or different and represent alkyl, allyl or alkoxyl groups containing from 1 to about 10 carbon atoms, and wherein m represents an integer from about 4 to about 10.
摘要:
F(CF2)n(CH2)mNH2 is produced in high yield, while reducing the amount of by-products contained in the reaction product and preventing the reactor from corroding. Provided is a process for producing a fluorinated alkylamine compound, which comprises reacting a compound represented by F(CF2)n(CH2)mX (wherein X represents a chlorine atom, a bromine atom or an iodine atom, and n and m each independently represents an integer of at least 1) with NH3 to produce a compound represented by F(CF2)n(CH2)mNH2 (wherein n and m have the same meanings as the above), and is characterized by conducting the reaction in the presence of a reaction solvent comprising an alkanediol as an essential component.
摘要:
The antifungal agent (E)-N-methyl-N-(1-naphthylmethyl)-6,6-dimethyl-hept-2-ene-4-ynyl-1-amine of formula (I) and acid addition salts thereof are prepared by reacting a chloro-compound of formula (IIIb) with a secondary amine of formula (II) in an aliphatic ketone-type solvent in the presence of a base and optionally iodide salt catalyst, and subsequently treating the resulting reaction mixture directly with aqueous hydrochloric acid to precipitate the hydrochloride of the compound of formula (I). The precipitate is separated, and the base of formula (I) can be liberated from the hydrochloride and can be converted into other pharmaceutically acceptable acid addition salts.
摘要:
Process technology for selectively isomerizing vinylidene olefin to tri-substituted olefin is described. The vinylidene olefin, normally in admixture with other types of olefins, especially linear 1-olefins, is treated with anhydrous hydrogen bromide under anhydrous conditions and in the absence of molecular oxygen and free radical initiator. The contacting period, which can be a matter of minutes, is sufficient to selectively isomerize the vinylidene olefin to tri-substituted olefin. If the process is conducted properly, little if any hydrobromination occurs.
摘要:
A preparation process of N,N′-dialkylalkanediamine by reacting dihaloalkane with lower alkylamine characterized by carrying out the reaction with controlling the residual amount in the reaction system of haloalkaneamine intermediate represented by the formula (4): wherein R is a lower alkyl group, R1 and R2 are a hydrogen atom or a lower alkyl group, X is a chlorine, bromine or iodine atom, and n is an integer of 2 to 6, and the invention inhibits formation of by-products cyclic dialkyldiamine and trialkylalkanetriamine and can provide desired N,N′-dialkylalkanediamine with a high yield.