JPS57192323A - Isoprenyl ether derivative - Google Patents

Isoprenyl ether derivative

Info

Publication number
JPS57192323A
JPS57192323A JP56076153A JP7615381A JPS57192323A JP S57192323 A JPS57192323 A JP S57192323A JP 56076153 A JP56076153 A JP 56076153A JP 7615381 A JP7615381 A JP 7615381A JP S57192323 A JPS57192323 A JP S57192323A
Authority
JP
Japan
Prior art keywords
compound
formula
reacted
group
formulai
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.)
Granted
Application number
JP56076153A
Other languages
Japanese (ja)
Other versions
JPS6366298B2 (en
Inventor
Yoshiyuki Tawara
Yasuhiro Komatsu
Hiroyasu Koyama
Reiko Kubota
Teruto Yamaguchi
Toshihiro Takahashi
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.)
Nisshin Seifun Group Inc
Original Assignee
Nisshin Seifun Group Inc
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
Application filed by Nisshin Seifun Group Inc filed Critical Nisshin Seifun Group Inc
Priority to JP56076153A priority Critical patent/JPS57192323A/en
Publication of JPS57192323A publication Critical patent/JPS57192323A/en
Publication of JPS6366298B2 publication Critical patent/JPS6366298B2/ja
Granted legal-status Critical Current

Links

Abstract

NEW MATERIAL:A compound of formulaI[n is 9 or 10; X is alkylene chain having an oxy bond or pendant OH group; Y is OH or NR2 (R is H or hydroxyethyl or two Rs together with the nitrogen atom forming an N'-hydroxyethyl substituted piperazine ring or phthalimide ring)]and an acid addition salt thereof.
EXAMPLE: Diethylene glycol monodecaprenyl ether.
USE: A viral infection inhibitor for vertebrate animals having antiviral and antitumor actions.
PROCESS: An isoprenyl alcohol of formula II is converted into a halide or arylsulfonic acid in a solvent, e.g. THF, at room temperature W100°C, and reacted with a compound of the formula MO-X-Y (M is alkali metallic atom) to give the compound of formulaI. A compound of formula III is reacted in the same way as described above to afford a compound of formula IV, which is then reacted with a compound of the formula NHR2 to give the compound of formulaIin which X is an alkylene group having pendant OH group.
COPYRIGHT: (C)1982,JPO&Japio
JP56076153A 1981-05-18 1981-05-18 Isoprenyl ether derivative Granted JPS57192323A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56076153A JPS57192323A (en) 1981-05-18 1981-05-18 Isoprenyl ether derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56076153A JPS57192323A (en) 1981-05-18 1981-05-18 Isoprenyl ether derivative

Publications (2)

Publication Number Publication Date
JPS57192323A true JPS57192323A (en) 1982-11-26
JPS6366298B2 JPS6366298B2 (en) 1988-12-20

Family

ID=13597075

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56076153A Granted JPS57192323A (en) 1981-05-18 1981-05-18 Isoprenyl ether derivative

Country Status (1)

Country Link
JP (1) JPS57192323A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8653131B2 (en) 2008-08-22 2014-02-18 Baxter Healthcare S.A. Polymeric benzyl carbonate-derivatives

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8653131B2 (en) 2008-08-22 2014-02-18 Baxter Healthcare S.A. Polymeric benzyl carbonate-derivatives
US8962549B2 (en) 2008-08-22 2015-02-24 Baxter International Inc. Polymeric benzyl carbonate-derivatives

Also Published As

Publication number Publication date
JPS6366298B2 (en) 1988-12-20

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