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ChemicalBook CAS DataBase List 4-CHLORO-1-METHYL-1H-QUINOLIN-2-ONE

4-CHLORO-1-METHYL-1H-QUINOLIN-2-ONE synthesis

9synthesis methods
-

Yield:32262-17-2 85%

Reaction Conditions:

Stage #1: 4-chloro-2(1H)-quinolinonewith sodium hydride in N,N-dimethyl-formamide at 0; for 0.166667 h;
Stage #2: methyl iodide in N,N-dimethyl-formamide at 0 - 20; for 3 h;

References:

Naik, Maruti;Humnabadkar, Vaishali;Tantry, Subramanyam J.;Panda, Manoranjan;Narayan, Ashwini;Guptha, Supreeth;Panduga, Vijender;Manjrekar, Praveena;Jena, Lalit Kumar;Koushik, Krishna;Shanbhag, Gajanan;Jatheendranath, Sandesh;Manjunatha;Gorai, Gopinath;Bathula, Chandramohan;Rudrapatna, Suresh;Achar, Vijayashree;Sharma, Sreevalli;Ambady, Anisha;Hegde, Naina;Mahadevaswamy, Jyothi;Kaur, Parvinder;Sambandamurthy, Vasan K.;Awasthy, Disha;Narayan, Chandan;Ravishankar, Sudha;Madhavapeddi, Prashanti;Reddy, Jitendar;Prabhakar;Saralaya, Ramanatha;Chatterji, Monalisa;Whiteaker, James;McLaughlin, Bob;Chiarelli, Laurent R.;Riccardi, Giovanna;Pasca, Maria Rosalia;Binda, Claudia;Neres, Jo?o;Dhar, Neeraj;Signorino-Gelo, Fran?ois;McKinney, John D.;Ramachandran, Vasanthi;Shandil, Radha;Tommasi, Ruben;Iyer, Pravin S.;Narayanan, Shridhar;Hosagrahara, Vinayak;Kavanagh, Stefan;Dinesh, Neela;Ghorpade, Sandeep R. [Journal of Medicinal Chemistry,2014,vol. 57,# 12,p. 5419 - 5434] Location in patent:supporting information