N,N-二烯丙基氨基甲酸叔丁酯置于grubbs Catalyst First Generation 间氯过氧苯甲酸体系中,用 二氯甲烷 用作溶剂,化学反应 21.0H,反应生成3-Boc-6-氧杂-3-氮杂二环[3.1.0]己烷 参考文献: 3-Hydroxypyrrolidine Inhibitors Of 5'-Methylthioadenosine Phosphorylase And Nucleosidase[fr] Inhibiteurs 3-Hydroxypyrrolidine De 5'-Méthylthioadénosine Phosphorylase Et Nucléosidase 标题: 3-Hydroxypyrrolidine Inhibitors Of 5'-Methylthioadenosine Phosphorylase And Nucleosidase[fr] Inhibiteurs 3-Hydroxypyrrolidine De 5'-Méthylthioadénosine Phosphorylase Et Nucléosidase 摘要:本发明涉及一般式(i)的3-羟基吡咯烷化合物,这些化合物是5'-甲硫腺苷磷酸化酶或5'-甲硫腺苷核苷酸酶的抑制剂.该发明还涉及在治疗希望抑制5'-甲硫腺苷磷酸化酶或5'-甲硫腺苷核苷酶的疾病或症状中使用这些化合物,包括癌症,并且涉及含有这些化合物的药物组合物.
专利号:WO-2025128848-A1 优先权日:2023-12-12 标题:Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use 发明人:HOUZE JONATHAN B; PANDYA BHAUMIK 权利人:VIGIL NEUROSCIENCE INC 摘要:The present disclosure provides compounds of Formula (I), useful for the activation of Triggering Receptor Expressed on Myeloid Cells 2 ('TREM2'). This disclosure also provides pharmaceutical compositions comprising the compounds, uses of the compounds, and compositions for treatment of, for example, a neurodegenerative disorder. Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula (I).
专利号:US-9937151-B2 优先权日:2010-06-18 标题 :Carbapenem antibacterials with gram-negative activity 发明人:CHOI WOO-BAEG; GRUSZECKA-KOWALIK EWA; JOO HYUNG-YEUL; LIU SHUANGPEI; MAO SHULI; LI YONGFENG; KIM DEOG-IL 权利人:FOB SYNTHESIS INC 摘要:The present invention provides β-methyl carbapenem compounds and pharmaceutical compositions useful in the treatment of bacterial infections and methods for treating such infections using such compounds and/or compositions. The invention includes administering an effective amount of a carbapenem compound or salt and/or prodrug thereof to a host in need of such a treatment.
专利号:US-9212161-B2 优先权日:2010-07-01 标 题:Chiral synthesis of pyrrolidine core compounds en route to neuronal nitric oxide synthase inhibitors
专利号:US-8518952-B2 优先权日:2008-08-06 标题 :6 substituted 2-heterocyclylamino pyrazine compounds as CHK-1 inhibitors 发明人:BRAGANZA JOHN FREDERICK; COLLINS MICHAEL RAYMOND; KATH JOHN CHARLES; NINKOVIC SACHA; LI HUI; RICHTER DANIEL TYLER 权利人:BRAGANZA JOHN FREDERICK; COLLINS MICHAEL RAYMOND; KATH JOHN CHARLES; NINKOVIC SACHA; LI HUI; RICHTER DANIEL TYLER; PFIZER 摘要:The present invention is directed to compounds of formula (I), n nand pharmaceutically acceptable salts thereof, their synthesis, and their use as CHK-1 inhibitors.