Methylation of 4-Aminoquinazoline 3-Oxide with Diazomethane
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چکیده
منابع مشابه
Synthesis and Characterization of Novel 4-oxo-1,4-dihydroquinoline-3-carboxamide Derivatives from Diazomethane and HCl
Reaction of thionyl chloride with 7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4- oxoquinoline-3-carboxylic acid 1 gave acid chloride 2. Compound 2 was reacted with glycine and D-glutamic acid to afford 2-(7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4- dihydroquinoline-3-carbonyl) aminopantandioicacid 3a and 2-(7-chloro-1-cyclopropyl-6- fluoro -4- oxo-1,4-dihydroquinoline-3-carbonyl)aminoacetica...
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A simple, efficient, and general method has been developed for the synthesis of various N-aryl heterocylic substituted-4-aminoquinazoline compounds from 4-chloro- quinazoline and aryl heterocyclic amines under microwave irradiation using 2-propanol as solvent. The advantages of the use of microwave irradiation in relation to the classical method were demonstrated.
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Efficient synthesis of 4-aminoquinazoline and thieno[3,2-d]pyrimidin-4-ylamine derivatives by microwave irradiation.
[reaction: see text] A simple, efficient, and high-yielding synthesis of quinazolin-4-ylamine and thieno[3,2-d]pyrimidin-4-ylamine derivatives is reported under microwave irradiation conditions. Reaction conditions including temperature, solvent, and reaction time have been studied. An efficient parallel workup procedure was developed to generate a small library (23 compounds) in a short time p...
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The treatment of silk with an ethereal solution of diazometbane result ed in a rapid decrease in tyrosine content, with no appreciable d ecrease in tensile strength <o f the fibers . The results indicate that the hydroxyl groups of tyrosine in the 'Untreated fibers are free. The total methoxyl content after treatment of the fiber for 25 hours or longer was greater than could be accounted for by...
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ژورنال
عنوان ژورنال: YAKUGAKU ZASSHI
سال: 1967
ISSN: 0031-6903,1347-5231
DOI: 10.1248/yakushi1947.87.5_578