摘要:
A process for the preparation of Pregabalin comprising: a) combining an alkali hydroxide and water, b) adding CMH at a temperature of about O° C to about 40° C; c) adding bromine, in a drop-wise manner, at a temperature of about O° C to about 40° C; d) heating; e) reacting with a strong mineral acid; f) extracting with a C4-8 alcohol, and g) mixing with a base to obtain Pregabalin. (Formula I)
摘要:
The present invention includes new salts of Raltegravir and crystalline forms thereof, pharmaceutical compositions containing the salts or crystalline forms, methods of using the salts or crystalline forms or the compositions to treat HIV infection or to prepare medicament for treating HIV infection, and a process for preparing Raltegravir potassium.
摘要:
The invention relates to pure (R)-CMH and to the optical resolution of CMH- racemate, a key intermediate in the synthesis of (S)-Pregabalin. The invention also relates to the process for optically purifying (R)-CMH and to the process for isolatin (S)-CMH from the mother liquor.
摘要:
The invention relates to pure (R)-CMH and to the optical resolution of CMH- racemate, a key intermediate in the synthesis of (S)-Pregabalin. The invention also relates to the process for optically purifying (R)-CMH and to the process for isolatin (S)-CMH from the mother liquor.
摘要:
Crystalline form of Pregabalin characterized by X-ray powder diffraction peaks at about 5.8, 18.4, 19.2, 20.7, and 23.7° 2θ ± 0.2° 2θ, methods for its preparation, its pharmaceutical compositions thereof, and methods for the preparation of crystalline form of Pregabalin characterized by X-ray powder diffraction peaks at about 5.7, 15.4, 17.2, 18.2, and 23.0° 2θ ± 0.2° 2θ, are provided.