ES414547A1 - A procedure for the preparation of a derivative of ampicillin. (Machine-translation by Google Translate, not legally binding) - Google Patents

A procedure for the preparation of a derivative of ampicillin. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES414547A1
ES414547A1 ES414547A ES414547A ES414547A1 ES 414547 A1 ES414547 A1 ES 414547A1 ES 414547 A ES414547 A ES 414547A ES 414547 A ES414547 A ES 414547A ES 414547 A1 ES414547 A1 ES 414547A1
Authority
ES
Spain
Prior art keywords
group
see formula
hydrogen atom
formula
ampicillin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
ES414547A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Yamanouchi Pharmaceutical Co Ltd
Original Assignee
Yamanouchi Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP4511872A external-priority patent/JPS5547036B2/ja
Priority claimed from JP8342472A external-priority patent/JPS4941396A/ja
Priority claimed from JP8510272A external-priority patent/JPS4942692A/ja
Priority claimed from JP8510372A external-priority patent/JPS4942693A/ja
Application filed by Yamanouchi Pharmaceutical Co Ltd filed Critical Yamanouchi Pharmaceutical Co Ltd
Publication of ES414547A1 publication Critical patent/ES414547A1/en
Expired legal-status Critical Current

Links

Abstract

A procedure for the preparation of an ampicillin derivative represented by the general formula **(See formula)** where R represents **(See formula)** where R1 represents a hydrogen atom, a methyl group or an ethyl group and A and B each represent a hydrogen atom, a hydroxy group, a methyl group, a methoxy group, a nitro group or a halogen atom, B can be combined with A on the carbon atom of position 3 to form a group **(See formula)** where Z represents -CH = N- or -CH = CH- and R2 represents a hydrogen atom, a hydroxy group, a phenyl group, a methyl group, a benzyl group, a methoxy group, an ethoxy group, a methylthio group, a trifluoromethyl group, a halogen atom, a nitro group, an acetyl group, an acetamido group, an ethoxycarbonyloxy group or a methylsulfonyl group, R2 can also form together with the group **(See formula)** a fused thiazolo, isothiazolo, pyrrolo, furo or benzo ring, which may be substituted with an oxo group, a methyl group or an acetyl group) and the dotted lines mean an arbitrary double bond, **(See formula)** where R3 and R4 each represent a hydrogen atom or a methyl group, **(See formula)** R5 represents a halogen atom, a methoxy group, a nitro group or a hydroxy group and R6 represents a hydrogen atom, a methoxy group, a halogen atom, a nitro group or a hydroxy group, or **(See formula)** where R7 represents a hydrogen atom or a hydroxy group, Y represents oxygen or sulfur and the dotted line means an arbitrary double bond, said substituent group being attached to the ampicillin molecule through a group -CO- in the positions 2, 3, 5 or 6 when the group = 0 is in position 4 and being attached to the ampicillin molecule through a group -CO- in positions 2, 4 or 5 when the group = 0 is in position 6; and you leave them; whose procedure consists in reacting the 6-aminopenicilanic acid derivatives represented by the formula **(See formula)** where D represents a hydrogen atom or **(See formula)** E represents a hydrogen atom or a group capable of being released under mild conditions, with a carboxylic acid represented by the formula **(See formula)** where R8 represents **(See formula)** when D is a hydrogen atom or R8 represents R when D is **(See formula)** or reactive derivatives thereof and releasing group E when said group is capable of being released under mild conditions. (Machine-translation by Google Translate, not legally binding)
ES414547A 1972-05-08 1973-05-08 A procedure for the preparation of a derivative of ampicillin. (Machine-translation by Google Translate, not legally binding) Expired ES414547A1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP4511872A JPS5547036B2 (en) 1972-05-08 1972-05-08
JP8342472A JPS4941396A (en) 1972-08-21 1972-08-21
JP8510272A JPS4942692A (en) 1972-08-25 1972-08-25
JP8510372A JPS4942693A (en) 1972-08-25 1972-08-25

Publications (1)

Publication Number Publication Date
ES414547A1 true ES414547A1 (en) 1977-01-16

Family

ID=27461645

Family Applications (1)

Application Number Title Priority Date Filing Date
ES414547A Expired ES414547A1 (en) 1972-05-08 1973-05-08 A procedure for the preparation of a derivative of ampicillin. (Machine-translation by Google Translate, not legally binding)

Country Status (1)

Country Link
ES (1) ES414547A1 (en)

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