METHOD OF SYNTHESIS OF IMIDAZOLES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALT Russian patent published in 1995 - IPC

Abstract RU 2028293 C1

FIELD: organic chemistry. SUBSTANCE: product of the general formula (I) : where R1 and R2 independently were taken from the order involving H, C1-C8-alkyl, unbranched C3-C8-alkyl, C3-C7-cycloalkyl, C4-C10-cycloalkylalkyl, C7-C14-aralkyl, 2-, 3- or 4-pyridinyl, 2-thienyl, 2-furanyl, phenyl substituted in definite cases with 1-3 groups. The latters were taken from the order involving F, Cl, Br, OH, C1-C4-alkoxy, C1-C4-alkyl, branched C3-C8-alkyl, CH3S(O)n,, NO2,, CF3, , CH3S(O)n or NR7R8; or R1 and R2 taken together form the group (I) where L - 0,0(CH2)m+1O or (CH2)m where m = 0-4; R3 - H, C1-C6-alkyl, allyl, benzyl or phenyl substituted in definite cases with F, Cl, CH3, CH3O or CF3; R4 - -C1-C8-alkyl with unbranched chain that is substituted with F, C3-C8-alkyl with branched chain, C3-C7-cycloalkyl, C4-C10-cycloalkylalkyl, C7-C14-aralkyl where aryl-group in definite cases is substituted with 1-3 groups. The latters were taken from the order involving C1-C4-alkyl or alkoxy-group, F, Br, Cl, NH2, OH, CN, , CF3, NO2, C1-C4-carboalkoxy, NR7R8 or NCOR7, C3-C6-alkenyl or alkinyl, C1-C3-perfluoroalkyl, phenyl substituted in definite cases with 1-3 groups. The latters were taken from C1-C4-alkyl, C1-C4-alkoxy, F, Br, Cl, NH2, OH, CN, CO2H, CF3, NO2, C1-C4-carboxy, NR7R8 or NCOR7, pentafluorophenyl, benzyl substituted in definite cases 1-3 groups taken from C1-C4-alkyl or alkoxy, F, Br, Cl, NH2, OH, CN, CO2H, CF3, NO2, C1-C4-carboalkoxy, NR7R8 or NCOR7: 2-, 3- or 4-pyridinyl, pyrimidinyl or biphenyl, S(O)n,O,NR5,CH2; R5 - H, C1-C6-alkyl or benzyl; R6 - H, C1-C8-alkyl, C3-C8-alkyl with branched chain, C3-C7-cycloalkyl, C3-C8-alkenyl or alkinyl, phenyl substituted in definite cases with 1-3 groups. The latters were taken from C1-C4-alkyl or alkoxy, F, Br, Cl, NH2, OH, CN, CO2H, CF3, NO2, C1-C4/ -carboalkoxy, NR7R8 or NCOR7, pentafluorophenyl, benzyl substituted in definite cases with 1-3 groups which were taken from C1-C4-alkyl or alkoxy, F, Br, Cl, NH2, OH, CN, CO2H, CF3, NO2, C1-C4-carboalkoxy, NR7R8 or NCOR7, R7 and R8 are independently, H and C1-C4-alkyl; A - C2-C10-alkyl, C3-C10-alkyl with branched chain, C3-C10-alkenyl, C3-C10-alkinyl; Y - O, S, H2, n = 0-2. Reagent 1: compound of the general formula: where R1,R2,R3,R6 - as indicated above. Reagent 2: isocyanate of the formula R4-N=C=O where R4 - as indicated above. EFFECT: improved method of synthesis. 6 tbl

Similar patents RU2028293C1

Title Year Author Number
METHOD OF SYNTHESIS OF IMIDAZOLE DERIVATIVES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS 1991
  • Dzheffri Tomas Billkhajmer[Us]
  • Piter Dzhon Dzhillis[Ca]
  • S.Ehnn Khajli[Us]
  • Tomas Piter Mehdeski
  • Rut Richmond Uehksler[Us]
RU2026292C1
NITROGEN-CONTAINING HETEROCYCLIC DERIVATIVES OF FLUORENE 1992
  • Vendell Vilki Vilkersehn[Us]
  • Kristofer Ehllehn Telena[Us]
RU2051151C1
CYCLIC UREAS, METHOD OF INHIBITION OF RETROVIRUS GROWTH AND PHARMACEUTICAL COMPOSITION 1992
  • Patrik Juk-Sun Lehm
  • Charl'Z Dzhozef Ajrmehnn
  • Karl Nikolas Khodzh
  • Prabkhakar Kondadzhi Dzhadkhav
  • Dzhordzh Vinsent Delukka
RU2131420C1
ISOXAZOLINES AND ISOXAZOLES, METHOD OF INHIBITION OF PLATELET AGGREGATION, PHARMACEUTICAL COMPOSITION INHIBITING PLATELET AGGREGATION 1994
  • Uitajak Dzhon
  • Z'Ju Chu-Bajao
  • Sileki-Dzurdz Tais Motria
  • Olson Richard Ehrik
  • Degrado Uill'Jam Frehnk
  • Kejn Gehri Ehjvonn
  • Vatt Duglas Gaj
  • Pinto Donald
RU2149871C1
IMIDAZOLE DERIVATIVES 1992
  • Dehvid Dzhon Karini[Us]
  • Dzhon Dzhonas Vitautas Dansia[Us]
  • Pankras Chor Bun Vong[Us]
RU2017733C1
ANTHRAPYRAZOLONE DERIVATIVES, METHODS OF THEIR SYNTHESIS AND METHODS OF SYNTHESIS OF ANTHRAPYRAZOLONES FROM THEIR SHOWING ANTITUMOR ACTIVITY 1994
  • Zang Lin-Khua
  • Auerbakh Dzhozef
RU2142456C1
CONDENSED HETEROCYCLIC COMPOUNDS 2006
  • Aso Kazujosi
  • Motizuki Mitijo
  • G'Jorkos Al'Bert Charl'Z
  • Korrett Kristofer Piter
  • Cho Suk Jang
  • Pratt Skott Alan
  • Sidem Kristofer Stefen
RU2408586C2
CYCLIC PEPTIDES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, PHARMACEUTICAL COMPOSITION 1992
  • Villijam Frehnk Degrado[Us]
  • Shehron Ehnn Dzhakson[Us]
  • Shehkehr Akhmed Mouza[Us]
RU2096415C1
1-N-ALKYL-N-ARYLPYRIMODINEAMINES, METHOD OF PATIENT TREATMENT, PHARMACEUTICAL COMPOSITION 1994
  • Oldrich Paul' Ehduard
  • Arvanitis Argajrios Dzhordzhios
  • Chizman Robert Skott
  • Chorvat Robert Dzhon
  • Kristos Tomas Judzhin
  • Gilligan Paul' Dzhozef
  • Grigoriadis Dmitrij Ehmil
  • Khodzh Karl Nikolas
  • Krenitski Paul' Dzhon
  • Skoulfild Ehverett Lejtem
  • Tam Sang Uill'Jam
  • Uasserman Zel'Da Rakovitts
RU2153494C2
POLYCYCLIC COMPOUNDS, THEIR DERIVATIVES, PHARMACEUTICAL PREPARATIONS AS ENHANCERS AND METHOD OF TREATMENT OF INTELLECTUAL ACTIVITY DISORDER 1994
  • Telekha Khristofer Allen
  • Vilkerson Vendell Vilki
  • Ierl Richard Alan
RU2152944C1

RU 2 028 293 C1

Authors

Dzheffri Tomas Billkhajmer[Us]

Piter Dzhon Dzhillis[Ca]

S.Ehnn Khajli[Us]

Tomas Piter Mehdeski

Rut Richmond Uehksler[Us]

Dates

1995-02-09Published

1989-12-04Filed