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Potassium Hydroxide → HCID 178506391, 화합물

HRID 2199507
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HRID 2199507 반응식
[Cl:1][C:2]1[C:11](I)=[CH:10][C:5]2[NH:6][C:7](=[S:9])[NH:8][C:4]=2[CH:3]=1.[OH-].[K+].[F:15][C:16]([F:19])([F:18])I>CN(C)C=O.C(OCC)(=O)C>[Cl:1][C:2]1[C:11]([C:5]2[CH:10]=[CH:11][C:2]([Cl:1])=[CH:3][CH:4]=2)=[CH:10][C:5]2[NH:6][C:7]([S:9][C:16]([F:19])([F:18])[F:15])=[N:8][C:4]=2[CH:3]=1
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6

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HCID 14797Potassium HydroxideHCID 16843TrifluoroiodomethaneHCID 574814685-Chloro-6-iodo-1H-benzo[d]imidazole-2(3H)-thione

생성물 1

HCID 178506391HCID 178506391, 화합물

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매

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온도
120 °C

실험 절차

Compound number 102 (i.e., 6-chloro-5-(4-chlorophenyl)-2-trifluoromethylthiobenzimidazole) was prepared as follows. A 250-mL 3-necked round-bottom flask was charged with a solution of 5-chloro-6-iodo-2,3-dihydro-1H-1,3-benzodiazole-2-thione (2 g, 6.44 mmol, 1.00 equiv) in N,N-dimethylformamide (100 mL) and potassium hydroxide (1.1 g, 3.00 equiv). Trifluoro(iodo)methane was introduced to the above. The resulting solution was stirred for 3 h at 120° C. in an oil bath. The resulting solution was diluted with 250 mL of ethyl acetate. The resulting mixture was washed with 3×200 mL of water and 2×200 mL of brine. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:10). This resulted in 400 mg (16%) of 5-chloro-6-iodo-2-[(trifluoromethyl)sulfanyl]-1H-1,3-benzodiazole as a yellow solid.

후처리

  1. washThe resulting mixture was washed with 3×200 mL of water and 2×200 mL of brine
  2. concentrationThe resulting mixture was concentrated under vacuum
  3. customThis resulted in 400 mg (16%) of 5-chloro-6-iodo-2-[(trifluoromethyl)sulfanyl]-1H-1,3-benzodiazole as a yellow solid

출처 및 근거

ORD 기록
ord-1a3c1a06ac424a49a57fd0ca3185f6a9
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09359305B2

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