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HCID 54512153, 화합물 → HCID 22008532, 화합물

HRID 321991
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HRID 321991 반응식
[CH:1](=[N:8][N:9]([C:21]1[CH:26]=[C:25]([Cl:27])[C:24]([CH2:28][C:29]2[CH:34]=[CH:33][C:32]([Cl:35])=[CH:31][CH:30]=2)=[C:23]([Cl:36])[CH:22]=1)[C:10]([NH:12][CH2:13]C(OCC)OCC)=[O:11])C1C=CC=CC=1>C(#N)C.Cl>[Cl:27][C:25]1[CH:26]=[C:21]([N:9]2[C:10](=[O:11])[NH:12][CH2:13][CH:1]=[N:8]2)[CH:22]=[C:23]([Cl:36])[C:24]=1[CH2:28][C:29]1[CH:34]=[CH:33][C:32]([Cl:35])=[CH:31][CH:30]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 54512153HCID 54512153, 화합물

생성물 1

HCID 22008532HCID 22008532, 화합물수율 95%

시약·촉매·용매 2

HCID 313Hydrochloric Acid촉매HCID 6342Acetonitrile용매

실험 절차

In 5 ml of acetonitrile was dissolved 0.4 g of 1-benzylidene-2-[4-(4-chlorobenzyl)-3,5-dichlorophenyl]-4-(2,2-diethoxyethyl)-semicarbazide. To the solution was added one drop of 35% hydrochloric acid. The mixture was stirred for one hour at room temperature. The reaction mixture was cooled, then resulting crystalline precipitate of the titled compound was collected by filtration. The yield was 95%. m.p.199-200° C.

후처리

  1. temperatureThe reaction mixture was cooled
  2. filtrationresulting crystalline precipitate of the titled compound was collected by filtration

출처 및 근거

ORD 기록
ord-8e77f65417904bfabe8315b4f7ddf77b
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06211178B1

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