Synthesis of Antischizophrenic Remoxipride
More Information
Abstract
Starting from 2,6 dihydroxyacetophenone, and undergoing methylation, oxidation, bromination and then amidation with S ( ) 2 aminomethyl 1 ethylpyrrolidine which was prepared from the raceme with D ( ) tartaric acid as resolving agent, we syn
Related Articles
[1] WU Mingming, FANG Lei, GOU Shaohua, CHEN Li. 以2-甲基-2-取代苯氧基丙酸为离去基团的铂(Ⅱ)配合物的合成、表征及细胞毒活性 [J]. Journal of China Pharmaceutical University, 2013, 44(4): 303-306. DOI: 10.11665/j.issn.1000-5048.20130403
[2] Attempted asymmetric synthesis of optically pure tetrabenazine [J]. Journal of China Pharmaceutical University, 2010, 41(4): 321-325.
[3] Synthesis of Lomerizine Dihydrochloride [J]. Journal of China Pharmaceutical University, 2002, (2): 86-88.
[4] Synthesis of Terbinafine [J]. Journal of China Pharmaceutical University, 2001, (1): 10-11.
[5] Studies on Synthesis of Leflunomide [J]. Journal of China Pharmaceutical University, 2000, (5): 10-11.
[6] Synthesis of Ritodrine [J]. Journal of China Pharmaceutical University, 2000, (3): 3-4.
[7] Synthesis of Dopexamine [J]. Journal of China Pharmaceutical University, 1999, (5): 328-331.
[8] The Synthesis of Ba m buterol [J]. Journal of China Pharmaceutical University, 1999, (4): 11-12.
[9] Synthesis of Oxendolone [J]. Journal of China Pharmaceutical University, 1997, (5): 8-11.
[10] Synthesis of Milrinone [J]. Journal of China Pharmaceutical University, 1996, (6): 59-60.