Butyl isocyanate → N-(n-butylcarbamoyl)-4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide

HRID 1638908노트

반응식

HRID 1638908 반응식
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][N:16]=2)[C:10]=1[S:11]([NH2:14])(=[O:13])=[O:12])=[O:5])[CH3:2].C(=O)([O-])[O-].[K+].[K+].[CH2:27]([N:31]=[C:32]=[O:33])[CH2:28][CH2:29][CH3:30]>CC(C)=O>[CH2:27]([NH:31][C:32]([NH:14][S:11]([C:10]1[N:9]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][N:16]=2)[N:8]=[CH:7][C:6]=1[C:4]([O:3][CH2:1][CH3:2])=[O:5])(=[O:13])=[O:12])=[O:33])[CH2:28][CH2:29][CH3:30]

참가 물질

5

반응물 3

HCID 8110Butyl isocyanateHCID 11430Potassium CarbonateHCID 140491554-Ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide

생성물 1

HCID 19839374N-(n-butylcarbamoyl)-4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide수율 95.2%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a 70 ml acetone mixture of 8.5 g of 4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide and 6.0 g of anhydrous potassium carbonate, added was 3.3 g of n-butylisocyanate at room temperature, followed by heating under reflux for 3 hours. After the reaction was completed, acetone was evaporated under reduced pressure, and then the residue was emptied into ice water to filter insolbles off, and then the filtrate was precipitated with hydrochloric acid. Crystals precipitated was filtered, washed with water and dried to obtain 10.8 g of N-(n-butylcarbamoyl)-4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide. m.p.: 180° to 181° C.

후처리

  1. additionadded
  2. customat room temperature
  3. temperatureby heating
  4. temperatureunder reflux for 3 hours
  5. customacetone was evaporated under reduced pressure
  6. filtrationto filter insolbles off, and then the filtrate
  7. customwas precipitated with hydrochloric acid
  8. customCrystals precipitated
  9. filtrationwas filtered
  10. washwashed with water
  11. customdried

출처 및 근거

ORD 기록
ord-f49a1aa730cb47e18a9058c083cdc71e
출처 데이터셋
uspto-grants-1989_11
특허 번호
US04881965

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