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乙酰氯 → HCID 67530107,化合物

HRID 17841
笔记
打印预览

反应方程式

HRID 17841 反应方程式
[C:1](Cl)(=[O:3])[CH3:2].[NH2:5][C:6]1[CH:20]=[CH:19][C:9]2[N:10]([CH:16]3[CH2:18][CH2:17]3)[CH:11]=[N:12][S:13](=[O:15])(=[O:14])[C:8]=2[CH:7]=1>O1CCOCC1>[C:1]([NH:5][C:6]1[CH:20]=[CH:19][C:9]2[N:10]([CH:16]3[CH2:17][CH2:18]3)[CH2:11][NH:12][S:13](=[O:15])(=[O:14])[C:8]=2[CH:7]=1)(=[O:3])[CH3:2]
参与物实验过程后处理来源与证据反应笔记

参与物

4

反应物 2

HCID 6367乙酰氯HCID 675289727-amino-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxide

产物 1

HCID 67530107HCID 67530107,化合物

试剂、催化剂与溶剂 1

HCID 312751,4-二氧六环溶剂

实验过程

Acetyl chloride (0.5 mL) is added to a solution of 7-amino-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxide (0.5 g), prepared in the Step above, in dioxane (20 mL) and stirring is carried out at ambient temperature for 16 hours. After removing the solvent by distillation under reduced pressure, the residue is taken up in water, and the precipitate, of 7-acetamido-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxide, is collected by filtration, washed with water and dried. It is used directly in a subsequent step, according to the procedure described in Step D of Example 1, in order to obtain the expected product.

后处理

  1. customAfter removing the solvent
  2. distillationby distillation under reduced pressure
  3. filtrationthe precipitate, of 7-acetamido-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxide, is collected by filtration
  4. washwashed with water
  5. customdried

来源与证据

ORD记录
ord-589de87b7a3f4586adf488e89c164d58
来源数据集
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
专利号
US07741320B2

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记