Water → 2-[Bis(4-acetoxyphenyl)methyl]-N-(2,4-dimethoxyphenyl)benzamide

HRID 36438

반응식

HRID 36438 반응식
[CH3:1][O:2][C:3]1[CH:9]=[C:8]([O:10][CH3:11])[CH:7]=[CH:6][C:4]=1[NH2:5].C(N(CC)CC)C.[C:19]([O:22][C:23]1[CH:28]=[CH:27][C:26]([CH:29]([C:39]2[CH:44]=[CH:43][C:42]([O:45][C:46](=[O:48])[CH3:47])=[CH:41][CH:40]=2)[C:30]2[CH:38]=[CH:37][CH:36]=[CH:35][C:31]=2[C:32](Cl)=[O:33])=[CH:25][CH:24]=1)(=[O:21])[CH3:20].O>C(Cl)Cl>[C:19]([O:22][C:23]1[CH:24]=[CH:25][C:26]([CH:29]([C:39]2[CH:40]=[CH:41][C:42]([O:45][C:46](=[O:48])[CH3:47])=[CH:43][CH:44]=2)[C:30]2[CH:38]=[CH:37][CH:36]=[CH:35][C:31]=2[C:32]([NH:5][C:4]2[CH:6]=[CH:7][C:8]([O:10][CH3:11])=[CH:9][C:3]=2[O:2][CH3:1])=[O:33])=[CH:27][CH:28]=1)(=[O:21])[CH3:20]

참가 물질

6

실험 절차

In 20 ml of methylene chloride were dissolved 1.08 g of 2,4-dimethoxyaniline and 4.5 ml of triethylamine. To this solution was dropwise added under ice cooling 20 ml of methylene chloride containing 3 g of 2-[bis(4-acetoxyphenyl)methyl]benzoyl chloride obtained in Reference Example 2. After stirring for 7 hours, water was added thereto. The organic layer was separated off, and the aqueous layer was extracted with chloroform. The chloroform layer was combined with the organic layer, and the combined organic layer was washed with 2N aqueous hydrochloric acid solution and dried over anhydrous magnesium sulfate. The resulting solution was concentrated under reduced pressure to give 2.6 g of the desired product (Compound 2) as an oily matter.

후처리

  1. customobtained in Reference Example 2
  2. customThe organic layer was separated off
  3. extractionthe aqueous layer was extracted with chloroform
  4. washthe combined organic layer was washed with 2N aqueous hydrochloric acid solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationThe resulting solution was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-17e1a6fc8d7f4900b476ff014efbe71c
출처 데이터셋
uspto-grants-1995_05
특허 번호
US05413997

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