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Thiophosgene → 5-isothiocyanato-N,N,4-trimethylpyridin-2-amine

HRID 1398860
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HRID 1398860 반응식
[C:1](Cl)(Cl)=[S:2].[CH3:5][N:6]([CH3:15])[C:7]1[CH:12]=[C:11]([CH3:13])[C:10]([NH2:14])=[CH:9][N:8]=1>O1CCCC1.C(=O)([O-])O.[Na+]>[N:14]([C:10]1[C:11]([CH3:13])=[CH:12][C:7]([N:6]([CH3:15])[CH3:5])=[N:8][CH:9]=1)=[C:1]=[S:2]
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참가 물질

5

반응물 2

HCID 10040ThiophosgeneHCID 22136281N2,N2,4-trimethylpyridine-2,5-diamine

생성물 1

HCID 866328825-isothiocyanato-N,N,4-trimethylpyridin-2-amine수율 70.3%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 516892Sodium Bicarbonate용매2회

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온도
0 °C

실험 절차

Thiophosgene (9.3 mL, 125 mmol) was added dropwise to a stirred mixture of N2,N2,4-trimethylpyridine-2,5-diamine (15.7 g) in tetrahydrofuran (100 mL) and saturated aqueous sodium hydrogen carbonate (150 mL) at 0° C., and the mixture was stirred at 0° C. for 2 hr. The mixture was diluted with saturated aqueous sodium hydrogen carbonate, and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was washed with n-hexane to give the title compound as a colorless powder (14.1 g, 73.0 mmol, 70% in 2 steps).

후처리

  1. extractionextracted with ethyl acetate
  2. washThe combined organic layer was washed with brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. washThe residue was washed with n-hexane

출처 및 근거

ORD 기록
ord-0a47aaf55c734cb9be8c7df4772da2ae
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901141B2

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