反应 #4165333
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-abc3d03156ef46b7ad744dacc41383ae暂无可渲染的结构数据
C1=COC=C1C(=O)Cl产品信息
3-呋喃甲酰氯(CAS 26214-65-3)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-abc3d03156ef46b7ad744dacc41383ae反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3e169714427b41dda58bd9d4f9bfb8ea反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-af448009c5504e899c85d3c39b3f0e08反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e06ba71bcf90421b9e98479c592e1252反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d2b05506fe134804874573c242cafcdb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8385ccb60ddd42a9a7ad6840c706fe8c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-903a1a6880cf47ffabc613326be2fbe3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Beginning with 0.015 gm (0.047 mMol) 5-amino-3-(1-(2-phenyleth-1-yl)-1,2,3,6-tetrahydropyridin-4-yl)pyrrolo[3,2-b]pyridine and 0.008 mL (0.061 mMol) 3-furoyl chloride, the title compound was prepared essentially by the procedure described in Example 7.
来源 ID: ord-53e3ff96b88e40449fa07c3dc3a992bf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Beginning with 0.015 gm (0.047 mMol) 5-amino-3-(1-(2-phenyleth-1-yl)piperidin-4-yl)pyrrolo[3,2-b]pyridine and 0.008 mL (0.061 mMol) 3-furoyl chloride, the title compound was prepared essentially by the procedure described in Example 7.
来源 ID: ord-87a342d4de3744408487dcd570501fd9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Beginning with 0.015 gm (0.061 mMol) 5-amino-3-(1-ethylpiperidin-4-yl)pyrrolo[3,2-b]pyridine and 0.010 mL (0.080 mMol) 3-furoyl chloride, the title compound was prepared essentially by the procedure described in Example 7.
来源 ID: ord-c3dbdb3659f34d54b31b0f21f5e811ab反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Beginning with 0.015 gm (0.047 mMol) 5-amino-3-(1-tert-butoxycarbonylpiperidin-4-yl)pyrrolo[3,2-b]pyridine and 0.008 mL (0.062 mMol) 3-furoyl chloride, the title compound was prepared.
来源 ID: ord-d561c712fc304126aaea3874930564d3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Beginning with 1.0 gm (4.3 mMol) 5-amino-3-(1-methylpiperidin-4-yl)pyrrolo[3,2-b]pyridine and 0.68 gm (5.2 mMol) 3-furoyl chloride, 0.85 gm (61%) of the title compound were prepared as an ivory crystalline solid essentially by the procedure described in Example 4.
来源 ID: ord-bbbf5f1a88fa41ba9b1b6e79708d4ae0PubChem 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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