Synthesis of ( S )-3-amino-benzo[ b ][1,4]oxazepin-4-one via Mitsunobu and S N Ar reaction for a first-in-class RIP1 kinase inhibitor GSK2982772 in clinical trials

التفاصيل البيبلوغرافية
العنوان: Synthesis of ( S )-3-amino-benzo[ b ][1,4]oxazepin-4-one via Mitsunobu and S N Ar reaction for a first-in-class RIP1 kinase inhibitor GSK2982772 in clinical trials
المؤلفون: Jae Uk Jeong, James Kang, Joseph J. Romano, Philip A. Harris, Xiaoyang Dong, Lara Kathryn Leister, Yunfeng Lan, Robert W. Marquis
المصدر: Tetrahedron Letters. 58:2306-2308
بيانات النشر: Elsevier BV, 2017.
سنة النشر: 2017
مصطلحات موضوعية: 0301 basic medicine, 03 medical and health sciences, 030104 developmental biology, 010405 organic chemistry, Chemistry, Nucleophilic aromatic substitution, Stereochemistry, Kinase, Organic Chemistry, Drug Discovery, 01 natural sciences, Biochemistry, 0104 chemical sciences
الوصف: Two new synthetic routes were developed to prepare the RIP1 kinase inhibitor clinical candidate GSK2982772 involving a key (S)-3-amino-benzo[b][1,4]oxazepin-4-one intermediate prepared via Mitsunobu and SNAr cyclization reactions. Both routes are practical and cost effective compared to the initial medicinal chemistry route and are also applicable to kilogram scale-up to support on-going clinical studies.
تدمد: 0040-4039
DOI: 10.1016/j.tetlet.2017.05.001
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::637de1387e4bf16986aa1ccee7c48b88
https://doi.org/10.1016/j.tetlet.2017.05.001
Rights: CLOSED
رقم الانضمام: edsair.doi...........637de1387e4bf16986aa1ccee7c48b88
قاعدة البيانات: OpenAIRE
الوصف
تدمد:00404039
DOI:10.1016/j.tetlet.2017.05.001