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Acetic Acid → 5-Fluoromethyl-7-methoxy-N-(2,6-dichlorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide

HRID 1111271
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HRID 1111271 반응식
C[Si](C)(C)[NH:3][C:4]1[C:9]([Cl:10])=[CH:8][CH:7]=[CH:6][C:5]=1[Cl:11].[F:14][CH2:15][C:16]1[CH:21]=[C:20](Cl)[N:19]2[N:23]=[C:24]([S:26](Cl)(=[O:28])=[O:27])[N:25]=[C:18]2[N:17]=1.CS(C)=O.[C:34](O)(=[O:36])C>C(#N)C.C(Cl)Cl>[F:14][CH2:15][C:16]1[CH:21]=[C:20]([O:36][CH3:34])[N:19]2[N:23]=[C:24]([S:26]([NH:3][C:4]3[C:9]([Cl:10])=[CH:8][CH:7]=[CH:6][C:5]=3[Cl:11])(=[O:28])=[O:27])[N:25]=[C:18]2[N:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 679Dimethyl SulfoxideHCID 143626792,6-Dichloro-N-trimethylsilylanilineHCID 146234725-Fluoromethyl-7-chloro-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonyl chloride

생성물 1

HCID 146234745-Fluoromethyl-7-methoxy-N-(2,6-dichlorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide

시약·촉매·용매 2

HCID 6342
Acetonitrile
용매
HCID 6344Dichloromethane용매

실험 절차

A solution containing 3.08 g (13.1 mmol) of N-trimethylsilyl-2,6-dichloroaniline and 1.50 g (5.26 mmol) of 5-fluoromethyl-7-chloro-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonyl chloride in 15 ml of dry acetonitrile was prepared and 0.075 ml (1.05 mmol) of dimethyl sulfoxide was added with stirring at ambient temperature. The mixture was allowed to react over 4 days and the resulting brown solution was then diluted with 150 ml of methylene chloride, washed with water, and dried over magnesium sulfate. The solvent was removed by evaporation under reduced pressure and replaced with hexane to obtain, after collection of the solids and drying, 1.80 g (84 percent of theory) of the 7-chloro analog of the title compound in about 80 percent purity. This was dissolved in 25 ml of dry methanol, the solution cooled to 0°-5° C. and a mixture of 1.70 g (7.89 mmol) of 25 weight percent sodium methoxide in methanol and 5 ml of methanol was added dropwise with stirring over a 10 min. period. The mixture was allowed to react for 10 min. and then about 1 ml of acetic acid was added. The solid that formed was collected, washed with methanol and with water, and dried to obtain 1.15 g (54 percent of theory) of the title compound as a light brown solid. This was extracted by stirring in boiling methanol, cooling, collecting the solids, and drying to obtain 1.09 g of product melting at 189°-191° C. The proton and fluorine nmr spectra were compatible with the assigned structure.

후처리

  1. customwas prepared
  2. customto react over 4 days
  3. washwashed with water
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was removed by evaporation under reduced pressure
  6. customto obtain
  7. customafter collection of the solids
  8. customdrying
  9. dissolutionThis was dissolved in 25 ml of dry methanol
  10. temperaturethe solution cooled to 0°-5° C.
  11. additiona mixture of 1.70 g (7.89 mmol) of 25 weight percent sodium methoxide in methanol and 5 ml of methanol
  12. additionwas added dropwise
  13. stirringwith stirring over a 10 min. period
  14. customto react for 10 min.
  15. customThe solid that formed
  16. customwas collected
  17. washwashed with methanol and with water
  18. customdried

출처 및 근거

ORD 기록
ord-484bfe5c6e69428f8fad0145593a2bfd
출처 데이터셋
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04979981

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