反应 #3832047
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-9bb12b5d57854b9980d37d0846d9c555暂无可渲染的结构数据
C1COCCC1(CN)N产品信息
4-氨基甲基-2H-四氢吡喃-4-胺(CAS 50289-16-2)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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10 条反应 · 10 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9bb12b5d57854b9980d37d0846d9c555反应条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
来源 ID: ord-1c33dca907094ff3b418c6c1c05a23d0反应条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
来源 ID: ord-1c33dca907094ff3b418c6c1c05a23d0反应条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
来源 ID: ord-f8d23405ece94d8b8d6f5b564b708e93反应条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
来源 ID: ord-37ef2bbed1974d41ae20258cfd891311反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9bb12b5d57854b9980d37d0846d9c555反应条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
来源 ID: ord-fae9e5363a414d048386739003badf04反应条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
来源 ID: ord-1c33dca907094ff3b418c6c1c05a23d0反应条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
来源 ID: ord-f8d23405ece94d8b8d6f5b564b708e93反应条件: temp:110.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chloro-3-nitrobenzenesulfonamide, 4-(aminomethyl)tetrahydro-2H-pyran-4-amine, hydrochloric acid and triethylamine in dioxane (10 mL) was heated at 110° C. overnight. After cooling, the mixture was diluted with water (10 mL), and filtered. After cooling filtered
来源 ID: ord-37ef2bbed1974d41ae20258cfd891311PubChem References
以下资料来自该化合物的公开数据库参考记录。
