化工社
首页MCP工作台Skills
首页工作台通知我的
llms.txt · MCP 指南隐私政策 · 服务条款 · 支持v1.8.0
  1. 首页
  2. /反应

HCID 11381609,化合物 → HCID 59265141,化合物

HRID 646293
笔记
打印预览

反应方程式

HRID 646293 反应方程式
[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8]([NH2:10])=[O:9])=[CH:6][C:5]=1[C:13]([NH:15][C:16]1[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][CH:17]=1)=[O:14])([O-])=O.[H][H]>CO.[Pt]=O>[NH2:1][C:4]1[CH:12]=[CH:11][C:7]([C:8]([NH2:10])=[O:9])=[CH:6][C:5]=1[C:13]([NH:15][C:16]1[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][CH:17]=1)=[O:14]
参与物实验过程后处理来源与证据反应笔记

参与物

5

反应物 2

HCID 11381609HCID 11381609,化合物HCID 178418361HCID 178418361,化合物

产物 1

HCID 59265141HCID 59265141,化合物收率 99%

试剂、催化剂与溶剂 2

HCID 82844Platinum oxide (PtO)催化剂HCID 887Methanol溶剂

实验过程

4-Nitro-3-N-(4-chlorophenyl)-isophthalamide (46 mg) obtained in Example 1-2-20 was dissolved in 7 mL of methanol, and 10 mg of platinum oxide was added to the solution, followed by stirring the mixture for 30 minutes at room temperature in an atmosphere of hydrogen. The reaction mixture was filtered to remove insolubles, and the filtrate was concentrated under reduced pressure. The resulting solid was dried under reduced pressure to obtain 41 mg (99%) of 4-amino-3-N-(4-chlorophenyl)-isophthalamide.

后处理

  1. filtrationThe reaction mixture was filtered
  2. customto remove insolubles
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customThe resulting solid was dried under reduced pressure

来源与证据

ORD记录
ord-89f2ee8e4d8e440b9bedb14147e3fed3
来源数据集
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
专利号
US07705053B2

反应笔记

加载中…

本页导航参与物实验过程后处理来源与证据反应笔记