专利号:US-6198000-B1 优先权日:1997-07-07 标 题:Intermediates useful in the synthesis of quinoline antibiotics 发明人:HAWKINS JOEL M 权利人:PFIZER 摘要:A process for preparing a compound of the formula n wherein R 1 , m, o and p are described below, which comprises adding a base of the formula n wherein R 2 , R 3 and R 4 are as described below, to a solution comprising a compound of the formula n wherein R 1 , m, o and p are as described below, and a halonitromethane of the formula O 2 NCH 2 X, wherein X is a halogen atom dissolved in a non-aqueous inert solvent. The compounds of formula III are useful as intermediates in the syntheses of azabicyclo quinoline carboxylic acids, and their pharmaceutically acceptable salts and prodrugs, having antibacterial activity. This invention also relates to the base of formula IV wherein each R 2 is butyl, R 3 is hydrogen and each R 4 is t-butyl.
专利号:US-5298629-A 优先权日:1992-03-02 标题 :Intermediates in the synthesis of quinoline antibiotics 发明人:BRAISH TAMIN F 权利人:PFIZER 摘要:This invention relates to compounds of the formulae ##STR1## wherein R and X are defined as below. These compounds are useful as intermediates in the syntheses of azabicyclo quinoline carboxylic acids having antibacterial activity.
专利号:US-6057455-A 优先权日:1996-07-09 标题 :Preparation of intermediates useful in the synthesis of quinoline antibiotics 发明人:HAWKINS JOEL M 权利人:PFIZER 摘要:A process for preparing a compound of the formula ##STR1## wherein R 1 , m, o and p are described below, which comprises adding a base of the formula ##STR2## wherein R 2 , R 3 and R 4 are as described below, to a solution comprising a compound of the formula ##STR3## wherein R 1 , m, o and p are as described below, and a halonitromethane of the formula O 2 NCH 2 X, wherein X is a halogen atom dissolved in a non-aqueous inert solvent. The compounds of formula III are useful as intermediates in the syntheses of azabicyclo quinoline carboxylic acids, and their pharmaceutically acceptable salts and prodrugs, having antibacterial activity. This invention also relates to the base of formula IV wherein each R 2 is butyl, R 3 is hydrogen and each R 4 is t-butyl.
专利号:EP-0818445-A1 优先权日:1996-07-09 标 题 :Preparation of intermediates useful in the synthesis of quinoline antibiotics 发明人:HAWKINS JOEL MICHAEL 权利人:PFIZER 摘要:A process for preparing a compound of the formulan nwherein R 1 , m, o and p are described below, which comprises adding a base of thenformulan nwherein R 2 , R 3 and R 4 are as described below, to a solution comprising a compoundnof the formula n nwherein R 1 , m, o and p are as described below, and a halonitromethane of the formulanO 2 NCH 2 X, wherein X is a halogen atom dissolved in a non-aqueous inert solvent.nThe compounds of formula III are useful as intermediates in the syntheses of azabicyclonquinoline carboxylic acids, and their pharmaceutically acceptable salts and prodrugs,nhaving antibacterial activity. This invention also relates to the base of formula IVnwherein each R 2 is butyl, R 3 is hydrogen and each R 4 is t -butyl.
专利号:US-5256791-A 优先权日:1992-03-02 标 题 :Preparation of intermediates in the synthesis of quinoline antibiotics
专利号:CN-1076440-A 优先权日:1992-03-02 标题:Preparation of intermediates in the synthesis of quinoline antibiotics
摘要:H. G. Adolph and M. J. Kamlet, J. Am. Chem. Soc. 88, 4761 (1966). 参考文献:10.1021/jp061100f 摘要:Shen Q, Brown JW, Malona JA, Cochran JC, Richardson AD. Molecular structure and conformation of chloronitromethane as determined by gas-phase electron diffraction and theoretical calculations. J Phys Chem A. 2006 Jun 15;110(23):7491–5. doi: 10.1021/jp061100f.