Efficient one-pot synthesis of N-substituted 2-aminochromones, their benzo-fused derivatives, and diaminobenzodipyrandiones of two new structural classes

Synthesis

Volumn , Issue 5, 2010, Pages 849-857

  Roma, Giorgio ^a   Piras, Daniela ^a   Di Braccio, Mario ^a   Grossi, Giancarlo ^a  

^a UNIVERSITY OF GENOA   (Italy)

Author keywords

Amines; Chromones; Heterocycles; One pot synthesis; Pyrans

Indexed keywords

AMINOCHROMONES; CHROMONES; HETEROCYCLES; HIGH YIELD; ONE-POT SYNTHESIS; PHOSPHORYL CHLORIDE; SALICYLIC ACIDS; STRUCTURAL CLASS;

ACIDS; AMINES; CHLORINE COMPOUNDS; SUBSTITUTION REACTIONS;

SYNTHESIS (CHEMICAL);

1,2 DICHLOROETHANE; 2 (DIETHYLAMINO) 1H NAPHTHO[1,2 B]PYRAN 4 ONE; 2 (DIETHYLAMINO) 4H 1 BENZOPYRAN 4 ONE; 2 (DIETHYLAMINO) 4H NAPHTHO[1,2 B]PYRAN 4 ONE; 2 (DIETHYLAMINO) 4H NAPHTHO[2,3 B]PYRAN 4 ONE; 2 (DIMETHYLAMINO) 4H 1 BENZOPYRAN 4 ONE; 2 (DIMETHYLAMINO) 4H NAPHTHO[2,3 B]PYRAN 4 ONE; 2 (DIPROPYLAMINO) 4H 1 BENZOPYRAN 4 ONE; 2 (DIPROPYLAMINO) 4H NAPHTHO[1,2 B]PYRAN 4 ONE; 2 (PIPERIDIN 1 YL) 4H NAPHTHO[1,2 B]PYRAN 4 ONE; 2 (PYRROLIDIN 1 YL) 4H 1 BENZOPYRAN 4 ONE; 2 (PYRROLIDIN 1 YL) 4H NAPHTHO[2,3 B]PYRAN 4 ONE; 2 [METHYL(PHENYL)AMINO] 4H 1 BENZOPYRAN 4 ONE; 2,7 BIS(DIETHYLAMINO)BENZO[1,2 B:4,5 B']DIPYRAN 4,9 DIONE; 2,7 BIS(DIMETHYLAMINO)BENZO[1,2 B:4,5 B']DIPYRAN 4,9 DIONE; 2,7 BIS(DIPROPYLAMINO)BENZO[1,2 B:4,5 B']DIPYRAN 4,9 DIONE; 2,7 DIAMINOBENZO[1,2 B:4,5 B']DIPYRAN 4,9 DIONE DERIVATIVE; 2,8 BIS(DIETHYLAMINO) 4H,6H BENZO[1,2 B:4,5 B']DIPYRAN 4,6 DIONE; 2,8 BIS(DIPROPYLAMINO) 4H,6H BENZO[1,2 B:4,5 B']DIPYRAN 4,6 DIONE; 2,8 DIAMINO 4H,6H BENZO[1,2 B:5,4 B']DIPYRAN 4,6 DIONE DERIVATIVE; 4 CHLORO 2H NAPHTHO[2,3 B]PYRAN 2 ONE; ACETAMIDE; BENZOPYRAN DERIVATIVE; CHROMONE DERIVATIVE; PHOSPHORUS DERIVATIVE; PHOSPHORUS OXYCHLORIDE; PHTHALIC ACID DERIVATIVE; SALICYLIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION KINETICS; DRUG STRUCTURE; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; ONE POT SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 77955406533     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/S-0029-1218623     Document Type: Article

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