反应 #4176926
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-63b4b0633e3c4a3b94dedad17d3f11b5暂无可渲染的结构数据
C1=CC=C(C=C1)CC(C(C(=O)N)O)N中间体产品
3-amino-2-hydroxy-4-phenylbutanamide
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 | 3-amino-2-hydroxy-4-phenylbutanamide |
|---|---|
| English name | 3-amino-2-hydroxy-4-phenylbutanamide |
| IUPAC 名称 | — |
| CAS号 | 246856-66-6 |
| 数据库编号 | 13882355 |
| 分子式 | — |
| 分子量 | — |
产品信息
3-amino-2-hydroxy-4-phenylbutanamide(CAS 246856-66-6)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 13882355
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-63b4b0633e3c4a3b94dedad17d3f11b5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-baae0fcca55e4701b9a5d975d9430785反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (R)-5-oxo-1-(2,6-difluorobenzyl)-pyrrolidine-2-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide.
来源 ID: ord-714a9abe3e624e36bda24660fbc9b699反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (R)-5-oxo-1-(2-methoxy-6-trifluoromethyl-benzyl)-pyrrolidine-2-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide.
来源 ID: ord-9a0d4ed61089434c95d71491ee9756da反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (R)-5-oxo-1-(2-methoxy-6-trifluoromethyl-benzyl)-pyrrolidine-2-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide.
来源 ID: ord-9a0d4ed61089434c95d71491ee9756da反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (R)-5-oxo-1-pyridin-4-ylmethyl-pyrrolidine-2-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide using Dess Martin reagent.
来源 ID: ord-eba976035cf342f7a9db16e4644a2ba1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (R)-5-oxo-1-pyridin-4-ylmethyl-pyrrolidine-2-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide using Dess Martin reagent.
来源 ID: ord-eba976035cf342f7a9db16e4644a2ba1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (R)-1-(3,5-dimethoxy-benzyl)-5-oxo-pyrrolidine-2-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide.
来源 ID: ord-e625d59b025d4cefbde4bc54693976e0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (2R,4S)-1-Benzyl-4-methyl-5-oxo-pyrrolidine-2-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide.
来源 ID: ord-25b0d7d5328e48939ceb0397cd0d62fa反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (R)-3-Benzyl-1-methyl-2-oxo-imidazolidine-4-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide.
来源 ID: ord-e08012883cfa4f26a07e28ed26c27e8e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (R)-3-Benzyl-1-methyl-2-oxo-imidazolidine-4-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide.
来源 ID: ord-e08012883cfa4f26a07e28ed26c27e8e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Coupling of (R)-5-Oxo-1-(2-trifluoromethyl-benzyl)-pyrrolidine-2-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide.
来源 ID: ord-7a966723f58d48adaa930823433b8c38PubChem 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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