Patent classifications
C07C249/12
Process for the preparation of fluvoxamine maleate
The present invention relates to an industrially feasible and economically viable process for the preparation of fluvoxamine maleate of formula I. ##STR00001##
PROCESS FOR MAKING SIPONIMOD AND INTERMEDIATE THEREOF
The presented invention relates to a process for preparation of compound of formula (I) or a salt or a solvate thereof (i.e.) siponimod. The invention also relates to intermediates used in the process and solid forms of these intermediates.
##STR00001##
PROCESS FOR MAKING SIPONIMOD AND INTERMEDIATE THEREOF
The presented invention relates to a process for preparation of compound of formula (I) or a salt or a solvate thereof (i.e.) siponimod. The invention also relates to intermediates used in the process and solid forms of these intermediates.
##STR00001##
PROCESS FOR MAKING SIPONIMOD AND INTERMEDIATE THEREOF
The presented invention relates to a process for preparation of compound of formula (I) or a salt or a solvate thereof (i.e.) siponimod. The invention also relates to intermediates used in the process and solid forms of these intermediates.
##STR00001##
PROCESS FOR THE PREPARATION OF A KEY INTERMEDIATE OF SIPONIMOD
The present invention relates to a process for the preparation of a key intermediate and other intermediates useful for the synthesis of Siponimod, a drug used for the treatment of multiple sclerosis. Object of the invention are also said novel intermediates.
PROCESS FOR THE PREPARATION OF A KEY INTERMEDIATE OF SIPONIMOD
The present invention relates to a process for the preparation of a key intermediate and other intermediates useful for the synthesis of Siponimod, a drug used for the treatment of multiple sclerosis. Object of the invention are also said novel intermediates.
PROCESS FOR THE PREPARATION OF A KEY INTERMEDIATE OF SIPONIMOD
The present invention relates to a process for the preparation of a key intermediate and other intermediates useful for the synthesis of Siponimod, a drug used for the treatment of multiple sclerosis. Object of the invention are also said novel intermediates.
Efficient new process for synthesis of 2-amino-5-chloro-N,3-dimethylbenzamide
Described herein are novel methods of synthesizing 2-amino-5-chloro-N,3-dimethylbenzamide. Compounds prepared by the methods disclosed herein are useful for preparation of certain anthranilamide compounds that are of interest as insecticides, such as, for example, the insecticides chlorantraniliprole and cyantraniliprole. ##STR00001##
Efficient new process for synthesis of 2-amino-5-chloro-N,3-dimethylbenzamide
Described herein are novel methods of synthesizing 2-amino-5-chloro-N,3-dimethylbenzamide. Compounds prepared by the methods disclosed herein are useful for preparation of certain anthranilamide compounds that are of interest as insecticides, such as, for example, the insecticides chlorantraniliprole and cyantraniliprole. ##STR00001##
EFFICIENT NEW PROCESS FOR SYNTHESIS OF 2-AMINO-5-CHLORO-N-,3-DIMETHYLBENZAMIDE
Described herein are novel methods of synthesizing 2-amino-5-chloro-N,3-dimethylbenzamide. Compounds prepared by the methods disclosed herein are useful for preparation of certain anthranilamide compounds that are of interest as insecticides, such as, for example, the insecticides chlorantraniliprole and cyantraniliprole.
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