FIELD: chemistry.
SUBSTANCE: invention relates to a process for the preparation and purification of a compound of formula I or a salt thereof, which is an effective inhibitor for the treatment of mediated lymphocyte function-associated antigen-1 (LFA-1) diseases, comprising steps of: a) carrying out hydrolysis of the compound of formula AA: where R is a carbon-containing fragment, with a base in a two-phase medium; and b) isolating said compound of formula I or a salt thereof, said process further comprising purifying said compound of formula I by recrystallisation with an aqueous solution of acetone. .
EFFECT: technical result is the preparation of a compound of formula I with an optical purity of about 98%.
13 cl, 10 dwg, 1 tbl, 11 ex
Title |
Year |
Author |
Number |
INHIBITOR OF LYMPHOCYTE FUNCTION-ASSOCIATED ANTIGEN-1 (LFA-1), ITS PRODUCTION METHODS AND ITS POLYMORPH |
2013 |
- Zeller, Dzhejms, Robert
- Venkatraman, Sripati
- Brot, Elizabet, K.A.
- Ier, Subashri
- Kholl, Majkl
|
RU2778771C2 |
METHOD OF PRODUCING 1-(3, 4-DICHLOROBENZYL)-5-OCTYL BIGUANIDE OR SALT THEREOF |
2007 |
- Okaiti Josikhiko
- Tada Nobukhito
- Nomi Dajsuke
- Fudzita Nobukhisa
- Tsudzi Koiti
- Jamaguti Taizo
- Muguruma Jasuaki
- Tsudzimori Khisajuki
|
RU2440978C2 |
METHOD FOR PREPARING 1-(2S,3S)-2-BENZHYDRYL-N-(5-TERT-BUTYL-2-METHOCYBENZYL)QUINUCLIDIN-4-AMINE AS CAMPHOR SULFATE SALT, CITRATE SALT AND FREE BASE AND INTERMEDIATE COMPOUND |
2005 |
- Basford Patrisia Ehnn
- Post Ronald Dzhejms
- Smit Dzhulian Dunkan
- Tehjber Dzheral'Din Patrisija
|
RU2320659C9 |
METHOD OF OBTAINING HYDROCHLORIDE OF 1-(3,4-DICHLORO-2-FLUOROPHENYLAMINO)-7-METHOXYQUINAZOLIN-6-YLOXY)PIPERIDIN-1-YL)PROP-2-EN-1-ONE AND INTERMEDIATE COMPOUNDS, APPLIED IN IT |
2012 |
- Bang Keuk Chan
- Moon Joung Kho
- Chang Joung Kil
|
RU2563630C1 |
METHOD OF PREPARING DERIVATIVES OF 3-(TETRAZOL-5-YL)-1-AZAXANTHONE OR THEIR SALTS |
0 |
- Akira Nokhara
- Tosikhiro Isiguro
- Kiesi Ikava
|
SU858570A3 |
METHOD FOR PREPARING AND PURIFYING DERIVATIVES OF ERYTHROMYCIN |
2001 |
- Simizu Khitosi
- Tsuzaki Kaname
- Kurita Mitsukhiro
|
RU2248981C2 |
METHOD OF PREPARING CRYSTALLINE 7-[2-(2- AMINOTHIAZOLE-4-YL) -2(Z)-METHOXYIMINOACETAMIDO] -3-[(1- -METHYL -1-PYRROLIDINO) METHYL] -CEPH-3- EM-4-CARBOXYLATE DIHYDROCHLORIDE MONO- OR DIHYDRATE FREE FROM ANTIISOMER AND Δ-ISOMER |
1992 |
- Gari M.F. Lim[Us]
- Dzhon M. Roubaj[Us]
|
RU2039059C1 |
PHENYL AMINO PYRIMIDINE COMPOUND OR POLYMORPH OF SALT THEREOF |
2016 |
- Lyuj Binkhua
- Li Chenvej
- Syao Dan
|
RU2712226C2 |
PHOSPHONIC ACID ESTERS AND METHODS FOR SYNTHESIS THEREOF |
2011 |
- Uer Roj U.
- Elmond Merrik R.
- Lampert Bernkhard M.
|
RU2581045C2 |
N-(4-FLUOROBENZYL)-N-(1-METHYLPIPERIDIN-4-YL)-N'-(2-METHYLPROPYLOXY)PHENYLMETHYL) CARBAMIDE SALTS AND PREPARATION OF SAID SALTS |
2005 |
- Tjugesen Mikkel'
- Shlinger Natali
- Tol'F Bo-Ragnar
- Blatter Fritts
- Bergkhauzen Jorg
|
RU2387643C2 |