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HCID 54512153, 화합물 → HCID 22008532, 화합물

HRID 1604316
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인쇄 미리보기

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HRID 1604316 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-02487ef7e0be4bfd9759ec4cf944230b
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05994355

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