反应 #4129715
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a51a088f852744a698e7ca505ef8378d暂无可渲染的结构数据
CS(=O)(=O)C1CCNCC1产品信息
4-甲磺酰基-哌啶(CAS 290328-55-1)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a51a088f852744a698e7ca505ef8378d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f8369a3f21ff41a590b3a272e6fe986b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ad597dd4767d4ec6ab17969ee9e16f27反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e83f5636272749bc85755e8430176c61反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Reaction between 2-chloro-4-morpholin-4-yl-thieno[2,3-d]pyrimidine-6-carbaldehyde (General Procedure D-2) and 4-methanesulfonyl-piperidine (Example 34) using General Procedure B-3 yielded 2-chloro-6-(4-methanesulfonyl-piperidin-1-ylmethyl)-4-morpholin-4-yl-thieno[2,3-d]pyrimidine.
来源 ID: ord-539341d2bdb542a9a22dbee66b7b4645反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Reaction between 2-chloro-4-morpholin-4-yl-thieno[2,3-d]pyrimidine-6-carbaldehyde (General Procedure D-2) and 4-methanesulfonyl-piperidine (Example 34) using General Procedure B-3 yielded 2-chloro-6-(4-methanesulfonyl-piperidin-1-ylmethyl)-4-morpholin-4-yl-thieno[2,3-d]pyrimidine.
来源 ID: ord-9d337015a9444a02be091a5c11e86dfb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared from 4-(methylsulfonyl)piperidine (0.515 g, 3.16 mmol) and (2-chloropyrimidin-5-yl)boronic acid (0.5 g, 3.16 mmol) in accordance with General Method C to give the title compound as an off-white semi-solid. HPLC-MS: m/z MH+ 286.2, RT 0.17 minutes.
来源 ID: ord-f3674d9d3b4c4a319438e6d541bf6878反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Reaction between 2-chloro-4-morpholin-4-yl-thieno[2,3-d]pyrimidine-6-carbaldehyde (General Procedure D-2) and 4-methanesulfonyl-piperidine (Example 34) using General Procedure B-3 yielded 2-chloro-6-(4-methanesulfonyl-piperidin-1-ylmethyl)-4-morpholin-4-yl-thieno[2,3-d]pyrimidine.
来源 ID: ord-539341d2bdb542a9a22dbee66b7b4645反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Reaction between 2-chloro-4-morpholin-4-yl-thieno[2,3-d]pyrimidine-6-carbaldehyde (General Procedure D-2) and 4-methanesulfonyl-piperidine (Example 34) using General Procedure B-3 yielded 2-chloro-6-(4-methanesulfonyl-piperidin-1-ylmethyl)-4-morpholin-4-yl-thieno[2,3-d]pyrimidine.
来源 ID: ord-539341d2bdb542a9a22dbee66b7b4645反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a51a088f852744a698e7ca505ef8378d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f8369a3f21ff41a590b3a272e6fe986b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ad597dd4767d4ec6ab17969ee9e16f27PubChem References
以下资料来自该化合物的公开数据库参考记录。
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