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Thionyl Chloride → 5-Methoxy-1,3-dimethyl-1H-pyrazole-4-sulfonyl chloride

HRID 1031329
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HRID 1031329 반응식
[CH3:1][N:2]1[C:6]([O:7][CH3:8])=[CH:5][C:4]([CH3:9])=[N:3]1.S(Cl)(Cl)=O.[Cl:14][S:15](O)(=[O:17])=[O:16]>>[CH3:1][N:2]1[C:6]([O:7][CH3:8])=[C:5]([S:15]([Cl:14])(=[O:17])=[O:16])[C:4]([CH3:9])=[N:3]1
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참가 물질

4

반응물 3

HCID 24386Thionyl ChlorideHCID 24638Chlorosulfonic acidHCID 5810655-methoxy-1,3-dimethyl-1H-pyrazole

생성물 1

HCID 151369135-Methoxy-1,3-dimethyl-1H-pyrazole-4-sulfonyl chloride

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온도
5 °C

실험 절차

Into 70 ml of chlorosulfonic acid was added dropwise under cooling at 5° C. or lower 12.6 g (0.1 mol) of 1,3-dimethyl-5-methoxypyrazole. After the addition, the mixture was stirred at 100° C. for 8 hours. Then, the reaction mixture was cooled to 80° C., followed by dropwise addition of 11.9 g (0.1 mol) of thionyl chloride over 30 minutes. After the dropwise addition, the mixture was stirred at 100° C. for 2 hours. The reaction mixture was cooled and poured carefully into ice-water, whereby crude 1,3-dimethyl-5-methoxy-pyrazole-4-sulfonylchloride was formed as crystals The crystals were separated by filtration, dissolved in 20 ml of tetrahydrofuran and the resultant solution was added dropwise into 100 ml of aqueous ammonia (28%) at 10° C. or lower. After the addition, the mixture was stirred at room temperature for 30 minutes. The reaction mixture was evaporated under reduced pressure to remove low boiling components, whereby crystals were precipitated. The crystals were filtered, washed with water and dried to give 11.5 g of 1,3-dimethyl-5-methoxypyrazole-4-sulfonamide melting at 144°-146° C.

후처리

  1. additionAfter the addition
  2. temperatureThen, the reaction mixture was cooled to 80° C.
  3. additionAfter the dropwise addition
  4. stirringthe mixture was stirred at 100° C. for 2 hours
  5. temperatureThe reaction mixture was cooled

출처 및 근거

ORD 기록
ord-39e577f42d744c1ab526b37152022896
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04954164

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