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Quinazoline 4-alkyl-, basicity

Support-bound quinazolin-2,4-diones can be N-alkylated, either with alkyl halides under basic conditions or with aliphatic alcohols by means of the Mitsunobu reaction (Entries 12-14, Table 15.29). The methyl group of a 2-methylquinazolin-4-one is sufficiently acidic to undergo aldol condensations with aldehydes [343]. Aminations of chloroquinazolines are discussed in Section 10.1.2. [Pg.441]

Quinazoline methiodide, 29 Quinazoline 3-oxides, 31 Quinazoline-thiones, 31, 51 4-Quinazolone, 3-alkyl-, 31 Quindolines, 103, 134, 144, 146 Quindoline-11-carboxylic acid, 144 Quinindoline, 135, 144 Quinolines, alkoxy-, reactions of, 311 2-alkyl-, reaction with carbenes, 77 aza-effects in, 318 basicity of, 244, 245, 247, 288, 289... [Pg.216]


See other pages where Quinazoline 4-alkyl-, basicity is mentioned: [Pg.69]    [Pg.234]    [Pg.230]    [Pg.628]    [Pg.69]    [Pg.234]    [Pg.69]    [Pg.4]    [Pg.35]    [Pg.80]    [Pg.87]    [Pg.234]    [Pg.264]    [Pg.126]   
See also in sourсe #XX -- [ Pg.20 ]




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