5-bromo-6-nitro-2-(N-tert-butyloxycarbonylpiperazin-1-yl)quinoline | 159532-01-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 5-bromo-6-nitro-2-(N-tert-butyloxycarbonylpiperazin-1-yl)quinoline
• 英文别名: 5-bromo-6-nitro-2-(1-tert-butylcarboxypiperazinyl)quinoline；Tert-butyl 4-(5-bromo-6-nitroquinolin-2-yl)piperazine-1-carboxylate
• CAS: 159532-01-1
• 化学式: C₁₈H₂₁BrN₄O₄
• 分子量: 437.293
• InChiKey: AGSDNIIFKJXQCL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  27
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  91.5
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  5-bromo-6-nitro-2-(N-tert-butyloxycarbonylpiperazin-1-yl)quinoline 在 二氯胺T 、 正丁基锂 、 磷酸 、 三丁基氯化锡 、 sodium iodide 作用下， 生成 5-iodo-6-nitro-2-(N-tert-butyloxycarbonylpiperazin-1-yl)quinoline
  参考文献：
  名称：

  Synthesis of 123I-and labelled 5-iodo-6-nitroquipazine

  摘要：

  报告了强效和选择性 5-羟色胺再摄取复合放射性配体 [123I]- 和 [125I]5-iodo-6- 硝基喹嗪（5-iodo-6-nitro-2-piperazinylquinoline）的合成。通过七步合成顺序，提供了 BOC 保护的 5-三丁基锡-6-硝基喹嗪前体，用于放射性碘化。合成结束时，123I 和 125I 的放射性碘化率分别为 40% 和 60%，得到的标记产物具有很高的比活度（分别大于 4000 和大于 2000 Ci/mmol）和放射化学纯度（大于 98%）。

  DOI：

  10.1002/jlcr.2580341003
• 作为产物：
  描述：

  5-溴-2-氯喹啉 在 硫酸 、 硝酸 、 三乙胺 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 3.25h， 生成 5-bromo-6-nitro-2-(N-tert-butyloxycarbonylpiperazin-1-yl)quinoline
  参考文献：
  名称：

  Synthesis of 123I-and labelled 5-iodo-6-nitroquipazine

  摘要：

  报告了强效和选择性 5-羟色胺再摄取复合放射性配体 [123I]- 和 [125I]5-iodo-6- 硝基喹嗪（5-iodo-6-nitro-2-piperazinylquinoline）的合成。通过七步合成顺序，提供了 BOC 保护的 5-三丁基锡-6-硝基喹嗪前体，用于放射性碘化。合成结束时，123I 和 125I 的放射性碘化率分别为 40% 和 60%，得到的标记产物具有很高的比活度（分别大于 4000 和大于 2000 Ci/mmol）和放射化学纯度（大于 98%）。

  DOI：

  10.1002/jlcr.2580341003

文献信息

• Synthesis, radiolabeling and preliminary biological evaluation of radiolabeled 5-methyl-6-nitroquipazine, a potential radioligand for the serotonin transporter
  作者：Johan Sandell、Meixiang Yu、Patrick Emond、Lucette Garreau、Sylvie Chalon、Kjell Någren、Denis Guilloteau、Christer Halldin

  DOI：10.1016/s0960-894x(02)00787-4

  日期：2002.12

  potent and selective serotonin transporter inhibitor 6-nitroquipazine was synthesized and radiolabeled with tritium and the positron emitter carbon-11. [3H]5-methyl-6-nitroquipazine was found to have a K(d)=51+/-7 pM. The high affinity and the facile labeling of [11C]5-methyl-6-nitroquipazine makes it a promising radioligand for visualization of the serotonin transporter with positron emission tomography

  合成了5-甲基-6-硝基喹嗪，它是强效且选择性的5-羟色胺转运蛋白抑制剂6-硝基喹嗪的新型类似物，并用tri和正电子发射体carbon-11进行了放射性标记。发现[3 H] 5-甲基-6-硝基quipazine具有K（d）＝ 51 +/- 7pM。[11C] 5-甲基-6-硝基喹嗪的高亲和力和易标记性使其成为使用正电子发射断层显像可视化5-羟色胺转运蛋白的有前途的放射性配体。
• Synthesis of a fluorine-18-labelled derivative of 6-nitroquipazine, as a radioligand for the In vivo serotonin transporter imaging with PET
  作者：Mylène Karramkam、Frédéric Dollé、Héric Valette、Laurent Besret、Yann Bramoullé、Françoise Hinnen、Françoise Vaufrey、Carine Franklin、Sébastien Bourg、Christine Coulon、Michèle Ottaviani、Marcel Delaforge、Christian Loc'h、Michel Bottlaender、Christian Crouzel

  DOI：10.1016/s0968-0896(02)00098-6

  日期：2002.8

  Considerable efforts have been engaged in the design, synthesis and pharmacological characterization of radioligands for imaging the serotonin transporter, based on its implication in several neuropsychiatric diseases, Such as depression, anxiety and schizophrenia. In the 5-halo-6-nitroquipazine series, the fluoro derivative has been designed for positron emission tomography (PET). The corresponding 5-iodo-, 5-bromo- and 5-chloro N-Boc-protected quipazines as labelling precursors, as well as 5-fluoro-6-nitroquipazine as a reference compound have been synthesized. 5-[F-18]Fluoro-6-nitroquipazine has been radiolabelled with fluorine-18 (positron-emitting isotope, 109.8 min half-life) by nucleophilic aromatic substitution from the corresponding N-Boc protected 5-bromo- and 5-chloro-precursors using K[F-18]F-K-222 complex in DMSO by conventional heating (145degreesC, 2 min) or microwave activation (50 W, 30-45 s), followed by removal of the protective group with TFA. Typically, 15-25 mCi (5.5-9.2 GBq) of 5-[F-18]fluoro-6-nitroquipazine (1-2 Ci/mumol or 37-72 GBq/mumol) could be obtained in 70-80 min starting from a 550-650 mCi (20.3-24.0 GBq) aliquot of a cyclotron [F-18]F- production batch (2.7-3.8% non decay-corrected yield based on the starting [F-18]fluoride). Ex vivo studies (biodistribution in rat), as well as PET imaging (in monkey) demonstrated that 5-[(18)]fluoro-6-nitroquipazine ([F-18]-1d) readily crossed the blood brain barrier and accumulated in the regions rich in 5-HT transporter (frontal-and posterial cortex, striata). However, the low accumulation of the tracer in the thalamus (rat and monkey) as well as the comparable displacement of the tracer observed with both citalopram, a reference 5-HT re-uptake inhibitor and maprotiline, a norepinephrine re-uptake inhibitor (rat), indicate that 5-[F-18]fluoro-6-nitroquipazine ([F-18]-1d) does not have the suggested potential for PFT imaging of the serotin transporter (SERT). (C) 2002 Elsevier Science Ltd. All rights reserved.
• Sandell, J.; Yu, M.; Emond, P., Journal of labelled compounds and radiopharmaceuticals, 2001, vol. 44, p. S170 - S172
  作者：Sandell, J.、Yu, M.、Emond, P.、Gulyas, B.、Cselenyi, Z.、Sovago, J.、Garreau, L.、Hall, H.、Chalon, S.、Guilloteau, D.、Nagren, K.、et al.

  DOI：——

  日期：——
• Synthesis of 123I-and labelled 5-iodo-6-nitroquipazine
  作者：Chester A. Mathis、Joel D. Enas、Stephen M. Hanrahan、Eyup Akgün

  DOI：10.1002/jlcr.2580341003

  日期：1994.10

  The syntheses of the potent and selective serotonin reuptake complex radioligands [123I]- and [125I]5-iodo-6-nitroquipazine (5-iodo-6-nitro-2-piperazinylquinoline) are reported. A seven step synthetic sequence provided the BOC-protected 5-tributyltin-6-nitroquipazine precursor for radioiodination. End of synthesis radioiodination yields of ∼40% for 123I and ∼60% for 125I were achieved resulting in labelled products with high specific activities (>4000 and >2000 Ci/mmol, respectively) and radiochemical purities (>98%).

  报告了强效和选择性 5-羟色胺再摄取复合放射性配体 [123I]- 和 [125I]5-iodo-6- 硝基喹嗪（5-iodo-6-nitro-2-piperazinylquinoline）的合成。通过七步合成顺序，提供了 BOC 保护的 5-三丁基锡-6-硝基喹嗪前体，用于放射性碘化。合成结束时，123I 和 125I 的放射性碘化率分别为 40% 和 60%，得到的标记产物具有很高的比活度（分别大于 4000 和大于 2000 Ci/mmol）和放射化学纯度（大于 98%）。