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Document Type and Number:
Japanese Patent JPH0460594
Kind Code:
B2
Abstract:
Compounds of the formula wherein R<1>, R<2> and R<3> are independently selected from hydrogen, C1-5 alkyl and Ph; and R<4> is HSO2, (C1-5 alkyl)sulfonyl, PhSO2, PhCOCH2SO2 or ZCH2COO in which Z is CH2I, CCl3, HSO2CH2, (C1-5 alkyl)sulfonylmethyl, PhSO2CH2, Ph or fluorenylmethyl. The compounds illustrated can be prepared by an 11-step process, starting from 4-chloro-3-nitrophenol and ether derivatives thereof. Many of the intermediates in this process are novel and have, as do the illustrated compounds, antibacterial activity. Novel intermediates have the formulae (I), (II), (III) or (IV> wherein R<5> is H, CH3, benzyl, allyl, CH3SCH2, CH3OCH2, CH3O- CH2CH2OCH2, CCl3CH2, (C1-5 alkyl)3 SiCH2CH2 or Ph3SiCH2CH2; R<7> is CH3O, C2H5O, C1-5 alkyl or Ph; X is HSO3, (C1-5 alkyl) SO3, PhSO3, Cl, Br, I or OH; X' is as X (except OH, or CH3COO; X'' is as X, or CH3COO; and Y is H, NO2 or NH2.

Inventors:
UENDERU UIIRENJA
Application Number:
JP13424290A
Publication Date:
September 28, 1992
Filing Date:
May 25, 1990
Export Citation:
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Assignee:
UPJOHN CO
International Classes:
C07D209/10; A01N43/90; A61K31/40; A61K31/403; A61K31/404; A61P31/04; A61P35/02; C07C205/37; C07C205/39; C07C305/18; C07C309/65; C07C309/66; C07C309/73; C07C323/12; C07D209/12; C07D471/04; C07D487/04; C07D487/06; C07D487/10; C07F7/08