Some synthetic applications of 2,3-Dichloro-N-phenylmaleimide: A novel synthesis of 2-phenylpyrrolo[3,4-b]quinoxaline-1,3-diones. I
摘要:
2,3-Dichloro-N-phenylmaleimide 2 undergoes nucleophilic substitution reactions by a variety of nucleophiles giving either monosubstituted 5 or disubstituted 3 products. Treatment of 5 with sodium azide at room temperature results in cyclization to the corresponding 2-phenylpyrrolo[3,4-b]quinoxaline-1,3-diones 6, while at higher temperatures 5 is reduced to the 2-amino-3-amino-N-phenylmaleimides 7. (C) 1999 Elsevier Science Ltd. All rights reserved.
Katritzky, Alan R.; Fan, Wei-Qiang; Li, Qiao-Ling, Journal of Heterocyclic Chemistry, 1989, vol. 26, p. 885 - 892
作者:Katritzky, Alan R.、Fan, Wei-Qiang、Li, Qiao-Ling、Bayyuk, Shibli
DOI:——
日期:——
KATRIZKY, ALAN R.;FAN, WEI-QIANG;LI, QIAO-LING;BAYYUK, SHIBLI, J. HETEROCYCL. CHEM., 26,(1989) N, C. 885-892
作者:KATRIZKY, ALAN R.、FAN, WEI-QIANG、LI, QIAO-LING、BAYYUK, SHIBLI
DOI:——
日期:——
CASEIN KINASE 1delta (CK 1delta) INHIBITORS AND THEIR USE IN THE TREATMENT OF NEURODEGENERATIVE DISEASES SUCH AS TAUOPATHIES
申请人:Electrophoretics Limited
公开号:US20160354375A1
公开(公告)日:2016-12-08
The invention relates to pharmaceutical compositions comprising casein kinase 1 delta (CK1δ) and to the use of said inhibitors in the treatment of neurodegenerative disorders such as Alzheimer's disease.
Some synthetic applications of 2,3-Dichloro-N-phenylmaleimide: A novel synthesis of 2-phenylpyrrolo[3,4-b]quinoxaline-1,3-diones. I
2,3-Dichloro-N-phenylmaleimide 2 undergoes nucleophilic substitution reactions by a variety of nucleophiles giving either monosubstituted 5 or disubstituted 3 products. Treatment of 5 with sodium azide at room temperature results in cyclization to the corresponding 2-phenylpyrrolo[3,4-b]quinoxaline-1,3-diones 6, while at higher temperatures 5 is reduced to the 2-amino-3-amino-N-phenylmaleimides 7. (C) 1999 Elsevier Science Ltd. All rights reserved.