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Sulfuryl chloride → 5-t-Butyl-4-chloro-3-propionylaminopyrazole

HRID 2164504
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HRID 2164504 반응식
[C:1]([C:5]1[NH:9][N:8]=[C:7]([NH:10][C:11](=[O:14])[CH2:12][CH3:13])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].S(Cl)([Cl:18])(=O)=O>C(Cl)(Cl)Cl>[C:1]([C:5]1[NH:9][N:8]=[C:7]([NH:10][C:11](=[O:14])[CH2:12][CH3:13])[C:6]=1[Cl:18])([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24648Sulfuryl chlorideHCID 13235938N-(5-tert-Butyl-1H-pyrazol-3-yl)propanamide

생성물 1

HCID 132359475-t-Butyl-4-chloro-3-propionylaminopyrazole

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

5.8 g (0.03 mole) of 5-t-butyl-3-propionylaminopyrazole prepared in Example 5 was dispersed in 30 ml of chloroform, and the dispersion was stirred while adding dropwise thereto sulfuryl chloride. The mixture was further heated under reflux conditions for one hour, and the solvent was distilled off. To the residue was added a sodium bicarbonate aqueous solution whereby crystals were precipitated. The crystals were collected by filtration, washed with water and then dried to obtain 3.9 g of 5-t-butyl-4-chloro-3-propionylaminopyrazole. This product was recrystallized from hydrous methanol and found to have a melting point of 136° to 137° C.

후처리

  1. additionwhile adding dropwise
  2. temperatureThe mixture was further heated under reflux conditions for one hour
  3. distillationthe solvent was distilled off
  4. additionTo the residue was added a sodium bicarbonate aqueous solution whereby crystals
  5. customwere precipitated
  6. filtrationThe crystals were collected by filtration
  7. washwashed with water
  8. customdried

출처 및 근거

ORD 기록
ord-654a43e769e34dd6a1d9dae1ac83719c
출처 데이터셋
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04505739

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