142141-40-0Relevant articles and documents
Regioselective N-alkylation of 2-aminobenzylamine via chelation to 9- BBN
Bar-Haim, Galia,Kol, Moshe
, p. 2643 - 2644 (1998)
A selective synthesis of 2-amino-N-alkylbenzylamines by direct mono alkylation of 2-aminobenzylamine is achieved by a potassium tert- butoxide/alkyl halide treatment of a 9-BBN amine-aminoborane chelate.
Syntheses of 3,4- and 1,4-dihydroquinazolines from 2-aminobenzylamine
Díaz, Jimena E.,Ranieri, Silvia,Gruber, Nadia,Orelli, Liliana R.
supporting information, p. 1470 - 1477 (2017/08/02)
A straightforward strategy for the synthesis of dihydroquinazolines is presented, which allows for the preparation of 3,4- and 1,4-dihydroquinazolines with different substitution patterns from 2-aminobenzylamine (2-ABA) as common precursor. The required functionalization of both amino groups present in 2-ABA was achieved by different routes involving selective N-acylation and cesium carbonate-mediated N-alkylation reactions, avoiding protection/deprotection steps. The heterocycles were efficiently synthesized in short reaction times by microwave-assisted ring closure of the corresponding aminoamides promoted by ethyl polyphosphate (PPE).
NEW COMPOUNDS
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Page/Page column 22, (2009/01/24)
The present invention encompasses compounds of general Formula (I) wherein R2, R3, Q, W, X, Y and Z are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation