反应 #4156009
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-128a1b73e8e144d69af239fa967edb00暂无可渲染的结构数据
C1CCN(C1)C(=O)Cl产品信息
吡咯烷-1-碳酰氯(CAS 1192-63-8)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 70937
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-128a1b73e8e144d69af239fa967edb00反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-338b45ae59354d3683fd4fe493efe32d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c9495077160c4d069b35a5fe47c2c590反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c7d5abfbfd704828a40344ea9f4b7bcd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4aeef3b22bcd4285a93f78044360c835反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8a7e0d20f465436db6692b4b821416e5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ea9cae261a6549f8a742fd47f216e66a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f9cb14516b0d419f8f20b844c0f123e9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c45d1071da094e009f1fe6b92356176b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 1-Pyrrolidine carbonylchloride (1.10 g, 9.99 mmol) was dissolved in 400 ml if dichloromethane under N2. (Tert-butoxy)-N-(4-piperidyl)carboxamide (2.0 g, 9.99 mmol) and triethyl amine (1.40 mL, 9.99 mmol) were added and the reaction mixture was stirred for three days. The reaction was quenched with sat. NaHCO3 solution and extracted with dichlorormethane. The combined organic phases were dried over MgSO4 and the solvent evaporated to give the product as a white solid. (2.63 g, 8.84 mmol, 89%). The reaction was quenched with sat. NaHCO3 solution extracted with dichlorormethane The combined organic phases were dried over MgSO4 the solvent evaporated
来源 ID: ord-c6aef8e1c09949d59180d987f368afc7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This compound was prepared by using procedures analogous to those described for the synthesis of Example 85 starting from N-[3-(7-{1-[3-(cyanomethyl)azetidin-3-yl]-1H-pyrazol-4-yl}imidazo[1,2-b]pyridazin-3-yl)phenyl]-N′-(2,2,2-trifluoroethyl)urea and 1-pyrrolidinecarbonyl chloride. LCMS (M+H)+: m/z=593.2. This compound was prepared
来源 ID: ord-9ac8199fa1ad4242abf2e8681106d3b3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of N-{3-[7-(6-piperazin-1-ylpyridin-3-yl)imidazo[1,2-b]pyridazin-3-yl]phenyl}-N′-(2,2,2-trifluoroethyl)urea (20.5 mg, 0.0413 mmol) HCl salt, 1-pyrrolidinecarbonyl chloride (6.84 μL, 0.0619 mmol) and N,N-diisopropylethylamine (40.0 μL, 0.230 mmol) in DMSO (0.5 mL) was stirred at r.t. for 1 h. The mixture was diluted with DMSO, and purified by RP-HPLC (pH=10) to afford the desired product. LCMS (M+H)+: m/z=594.2. purified by RP-HPLC (pH=10)
来源 ID: ord-278bac378d8d4440bae46ff09f6183ddPubChem References
以下资料来自该化合物的公开数据库参考记录。
相关产品
12 related records
CAS 896103-65-4
CAS 1257992-23-6
CAS 51493-02-8
CAS 1174330-61-0
CAS 1696873-35-4
CAS 1383546-51-7
CAS 18739-38-3
CAS 1257992-29-2
CAS 75485-12-0
CAS 53670-57-8
CAS 168253-02-9
CAS 39539-66-7
