摘要:
An object of the present invention is to industrially advantageously produce N-nitroisoureas or a salt thereof which is useful as a synthetic intermediate for pharmaceuticals and pesticides. The present invention relates to a process for producing a compound represented by the formula (2):
wherein R 1 , R 2 and R 3 are as defined below, or a salt thereof, which comprises reacting a compound represented by the formula (1):
wherein R 1 represents an optionally substituted straight-chain or branched C 1 to C 6 alkyl group, R 2 and R 3 are the same or different and represent an optionally substituted straight-chain or branched C 1 to C 6 alkyl group, a cycloalkyl group or a substituted aryl group, or R 2 and R 3 simultaneously represent a hydrogen atom, or a salt thereof with a nitrating agent in the presence of sulfur trioxide.
摘要:
The invention relates to a method for the production of organic salts containing bis(perfluoroalkyl)phosphinate anions. According to said method, a tris(perfluoroalkyl)phosphine oxide is reacted with an alcohol and an organic base, which is stronger than the alcohol. The invention also relates to the salts which are produced according to said method and to the use thereof as ionic liquids.
摘要:
A trifluoroacetoxylation agent is disclosed which is safe and easy to handle, very useful in industry, and represented by the formula (1); wherein R 1 to R 4 are a substituted or unsubstituted, saturated or unsaturated alkyl group or a substituted or unsubstituted aryl group and can be the same or different, R 1 and R 2 and/or R 3 and R 4 can bond to form a nitrogen-containing ring, optionally containing one or more other hetero atoms, and R 1 and R 3 can bond to form a nitrogen-containing ring optionally containing one or more other hetero atoms. A preparation process for the agent is also provided.
摘要:
The invention relates to a method for the production of organic salts containing bis(perfluoroalkyl)phosphinate anions. According to said method, a tris(perfluoroalkyl)phosphine oxide is reacted with an alcohol and an organic base, which is stronger than the alcohol. The invention also relates to the salts which are produced according to said method and to the use thereof as ionic liquids.
摘要:
The present invention relates to the process for the preparation of the ACE inhibitor perindopril starting from stereospecific amino acid N-/1-(S)-ethoxy-carbonyl-butyl/-(S)-alanine which is activated with tetramethyluronium salts in the presence of tertiary organic base, following the reaction with (2S,3aS,7aS)-octahydroindolo-2-carboxylic acid or an ester thereof, and after completing the reaction followed by elimination of protective group by hydrogenation, phase transfer hydrogenation or extraction.
摘要:
O-Isopropylisourea hydrogen sulfate and O-isopropyl- isourea sulfate which are represented by the general formula (I); and a process for the production thereof: (I) [wherein X is HSO4 or 1/2SO4]. O-Isopropylisourea hydrogen sulfate can be produced by reacting cyanamide with isopropyl alcohol in the presence of sulfuric acid, and O-isopropylisourea hydrogen sulfate can be converted into O-isopropylisourea sulfate by neutralization with an alkali metal hydroxide.
摘要:
O-isopropyl-isourea hydrogen sulfate or sulfate represented by the formula (I): wherein X represents HSO 4 or 1/2 SO 4 and the production method thereof, wherein O-isopropyl-isourea hydrogen sulfate is obtained by reacting cyanamide and isopropyl alcohol in the presence of sulfuric acid and is neutralized with an alkali metal hydroxide to produce O-isopropyl-isourea sulfate.