JPS54100385A - 5-fluorouracil derivative and its preparation - Google Patents

5-fluorouracil derivative and its preparation

Info

Publication number
JPS54100385A
JPS54100385A JP614378A JP614378A JPS54100385A JP S54100385 A JPS54100385 A JP S54100385A JP 614378 A JP614378 A JP 614378A JP 614378 A JP614378 A JP 614378A JP S54100385 A JPS54100385 A JP S54100385A
Authority
JP
Japan
Prior art keywords
formula
fluorouracil
preparation
reaction
fluorouracil derivatives
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.)
Pending
Application number
JP614378A
Other languages
Japanese (ja)
Inventor
Masao Koyama
Masao Seki
Shunzo Fukatsu
Mitsuru Hisamatsu
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.)
Meiji Seika Kaisha Ltd
Original Assignee
Meiji Seika Kaisha 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
Application filed by Meiji Seika Kaisha Ltd filed Critical Meiji Seika Kaisha Ltd
Priority to JP614378A priority Critical patent/JPS54100385A/en
Publication of JPS54100385A publication Critical patent/JPS54100385A/en
Pending legal-status Critical Current

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

NEW MATERIAL:5-Fluorouracil derivatives of formula I (R is lower alkyl).
EXAMPLE: 1-(2'-chloro-1'-ethoxy)ethyl-5-fluorouracil.
USE: Anticarcinostatic agent or starting material of 5-fluorouracil derivatives. It is better in fat-soluble properties and the improvement in absorbability on oral administration and toxicity reduction is expected.
PREPARATION: The reaction between 2,4-bistrimethylsilyloxy-5-fluoropyrimidine and 1,2-dischloroethyl ether of formula II is conducted in a dilute solution of an organic solvent as dichloromethane or dioxane, then the reaction mixture is concentrated, under reduced pressure. Further the trimethylsilyl groups are eliminated by adding water to prepare the compound of formula I. The reaction proceeds at low temperature when a Lewis acid is added as a catalyst.
COPYRIGHT: (C)1979,JPO&Japio
JP614378A 1978-01-25 1978-01-25 5-fluorouracil derivative and its preparation Pending JPS54100385A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP614378A JPS54100385A (en) 1978-01-25 1978-01-25 5-fluorouracil derivative and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP614378A JPS54100385A (en) 1978-01-25 1978-01-25 5-fluorouracil derivative and its preparation

Publications (1)

Publication Number Publication Date
JPS54100385A true JPS54100385A (en) 1979-08-08

Family

ID=11630285

Family Applications (1)

Application Number Title Priority Date Filing Date
JP614378A Pending JPS54100385A (en) 1978-01-25 1978-01-25 5-fluorouracil derivative and its preparation

Country Status (1)

Country Link
JP (1) JPS54100385A (en)

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