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Carbon Disulfide → 5-Chloro-6-iodo-1H-benzo[d]imidazole-2(3H)-thione

HRID 1045093
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HRID 1045093 반응식
[OH-].[K+].[C:3](=[S:5])=S.[Cl:6][C:7]1[CH:8]=[C:9]([NH2:15])[C:10]([NH2:14])=[CH:11][C:12]=1[I:13]>O.CCO>[Cl:6][C:7]1[C:12]([I:13])=[CH:11][C:10]2[NH:14][C:3](=[S:5])[NH:15][C:9]=2[CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6348Carbon DisulfideHCID 14797Potassium HydroxideHCID 574814674-Chloro-5-iodobenzene-1,2-diamine

생성물 1

HCID 574814685-Chloro-6-iodo-1H-benzo[d]imidazole-2(3H)-thione

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

KOH (15.7 g, 238 mmol) in water (50 mL), followed by carbon disulfide (14.4 mL, 238 mmol), was added to a solution of 4-chloro-5-iodobenzene-1,2-diamine (50 g, 198 mmol) in EtOH (300 mL). The mixture was heated at reflux for 3 h, cooled and filtered. To the filtrate was added water (300 mL) and then AcOH (25 mL) in water (50 mL). The precipitate was collected, washed with water and a small amount of EtOH and dried to afford the desired product as a brown powder, which was used in the next step without further purification.

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 3 h
  3. temperaturecooled
  4. filtrationfiltered
  5. additionTo the filtrate was added water (300 mL)
  6. customThe precipitate was collected
  7. washwashed with water
  8. dry with materiala small amount of EtOH and dried

출처 및 근거

ORD 기록
ord-11312f24387c45d392369332a7e2839f
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08563746B2

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