JPS5543001A - Preparation of 2-amino-4,5-dicyanoimidazole - Google Patents

Preparation of 2-amino-4,5-dicyanoimidazole

Info

Publication number
JPS5543001A
JPS5543001A JP10631578A JP10631578A JPS5543001A JP S5543001 A JPS5543001 A JP S5543001A JP 10631578 A JP10631578 A JP 10631578A JP 10631578 A JP10631578 A JP 10631578A JP S5543001 A JPS5543001 A JP S5543001A
Authority
JP
Japan
Prior art keywords
cyanogen chloride
aqueous
dicyanoimidazole
amino
purity
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
JP10631578A
Other languages
Japanese (ja)
Inventor
Hideo Tanaka
Hisashi Suzuki
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.)
NITSUPOU KAGAKU KK
Nippoh Chemicals Co Ltd
Original Assignee
NITSUPOU KAGAKU KK
Nippoh Chemicals 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
Application filed by NITSUPOU KAGAKU KK, Nippoh Chemicals Co Ltd filed Critical NITSUPOU KAGAKU KK
Priority to JP10631578A priority Critical patent/JPS5543001A/en
Publication of JPS5543001A publication Critical patent/JPS5543001A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE: To obtain the title compound useful as a raw material for various medicines, in high yield and purity, by reacting diaminomaleonitrile with cyanogen chloride, using water as a reaction medium.
CONSTITUTION: One mole of diaminomaleonitrile is reacted with 1W1.5mol of cyanogen chloride in an aqueous medium, preferably at a temperature of -10W +80°C, to obtain 2-amino-4,5-dicyanoimidazole of the formula. Cyanogen chloride is preferably used in the form of an aqueous reaction mixture produced by blowing chlorine into an aqueous prussic acid. The resulting liquid adjusted to pH 0.1W7 after the reaction improves the purity of the product.
USE: Diazodicyanoimidazole produced by the diazotation of this compound is useful as a raw material for medicines, agricultural chemicals, and dyes.
COPYRIGHT: (C)1980,JPO&Japio
JP10631578A 1978-09-01 1978-09-01 Preparation of 2-amino-4,5-dicyanoimidazole Pending JPS5543001A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10631578A JPS5543001A (en) 1978-09-01 1978-09-01 Preparation of 2-amino-4,5-dicyanoimidazole

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10631578A JPS5543001A (en) 1978-09-01 1978-09-01 Preparation of 2-amino-4,5-dicyanoimidazole

Publications (1)

Publication Number Publication Date
JPS5543001A true JPS5543001A (en) 1980-03-26

Family

ID=14430535

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10631578A Pending JPS5543001A (en) 1978-09-01 1978-09-01 Preparation of 2-amino-4,5-dicyanoimidazole

Country Status (1)

Country Link
JP (1) JPS5543001A (en)

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