反应 #4168463
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-4829b8edf90c4d75934046013eb31c84暂无可渲染的结构数据
CC(C)(C)OC(=O)N1C2CCC1CNC2中间体产品
tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | 8-BOC-3,8-二氮杂双环[3.2.1]辛烷 |
|---|---|
| English name | tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate |
| IUPAC 名称 | — |
| CAS号 | 149771-44-8 |
| 数据库编号 | 15740908 |
| 分子式 | — |
| 分子量 | — |
产品信息
8-BOC-3,8-二氮杂双环[3.2.1]辛烷(CAS 149771-44-8)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 15740908
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-4829b8edf90c4d75934046013eb31c84反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f67c891f1599472092840dfcbba2159b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0cd9fdc7fc4740f98b3f0321d64b682a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6f733bc8c7d14ff996ad7dcf6392c269反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7cc8ac2540d54d19ab1cdfdfeb0f48e3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-afddc88a186441a5af95ba0a081aaca3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-be37eeca2ab64817bc6da98cbac590c9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c41f124256b3420090e8a1a34471cdad反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (2.5 g, 11.7 mmol) in CH2Cl2 (50 mL) was treated with trimethylsilyl isocyanate (14 mL, 117 mmol). The resultant mixture was stirred at rt for 4 h., concentrated and redissolved in CH2Cl2 (50 mL). To this solution was added HCl (4.0 N in 1,4-dioxane, 12 mL), and the resultant mixture was stirred at rt for 3 h. Concentration afforded the title compound as a white powder (2.4 g, 99%). MS (ESI): mass calcd. for C7H13N3O, 155.1; m/z found, 156.2 [M+H]+. concentrated redissolved in CH2Cl2 (50 mL) To this solution was added HCl (4.0 N in 1,4-dioxane, 12 mL) Concentration
来源 ID: ord-50ff139614284bd6b080f060091df286反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirred solution of acid VIII (0.00021 mol, 1 eq) in DMF (5 mL), EDCI (0.048 g, 0.00024 mol, 1.1 eq), HOBt (0.038 g, 0.00024 mol, 1.1 eq) and DIPEA (0.15 mL, 0.00078 mol, 2.5 eq) were added at 0° C. and stirred for 15 minutes. A solution of amine LXXI (0.00021 mol, 1 eq) was then added at 0° C. and then the resulting mixture was allowed to stir at room temperature for overnight. After completion of the reaction, water (20 mL) was added and extracted with ethyl acetate (2×30 mL). The combined organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel, 60-120 mess, 70% ethyl acetate in hexane) to give compound in 49-55% yield. to stir at room temperature for overnight was added extracted with ethyl acetate (2×30 mL) The combined organic layer was dried over anhydrous Na2SO4 concentrated under reduced pressure The crude product was purified by column chromatography (silica gel, 60-120 mess, 70% ethyl acetate in hexane) to give compound in 49-55% yield
来源 ID: ord-381f939f374b4261937448f12cd7e969反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4829b8edf90c4d75934046013eb31c84反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f67c891f1599472092840dfcbba2159bPubChem 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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