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Isoamyl Nitrite → 1-(2,4-Difluorophenyl)-N-ethyl-4-nitroso-1H-pyrazol-5-amine

HRID 383568
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HRID 383568 반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[N:9]1[C:13]([NH:14][CH2:15][CH3:16])=[CH:12][CH:11]=[N:10]1.[N:17](OCCC(C)C)=[O:18]>CCOC(C)=O.CCO.Cl.CC(O)C>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[N:9]1[C:13]([NH:14][CH2:15][CH3:16])=[C:12]([N:17]=[O:18])[CH:11]=[N:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 2

HCID 8053Isoamyl NitriteHCID 671980121-(2,4-difluorophenyl)-N-ethyl-1H-pyrazol-5-amine

생성물 1

HCID 866529991-(2,4-Difluorophenyl)-N-ethyl-4-nitroso-1H-pyrazol-5-amine

시약·촉매·용매 4

HCID 313Hydrochloric Acid용매HCID 702Ethanol용매HCID 3776Isopropanol용매
HCID 8857
Ethyl Acetate
용매

실험 절차

A solution of 1-(2,4-difluorophenyl)-N-ethyl-1H-pyrazol-5-amine (1.15 g, 5.16 mmol) in 4.0 mL of EtOAc, 2.0 mL of EtOH and 4.0 mL of 5-6 N HCl in 2-propanol was cooled in an ice/brine bath and treated with isoamyl nitrite (0.70 mL, 5.28 mmol) drop wise. After stirring at this temperature for 15 min, the reaction was quenched by the addition of 28-30% NH4OH solution and EtOAc, forming a deep blue solution. The EtOAc layer was separated, washed with brine, dried and concentrated to afford the title compound as a brown crystalline solid. MS (ES+): 253.1 (M+H)+.

후처리

  1. customthe reaction was quenched by the addition of 28-30% NH4OH solution and EtOAc
  2. customforming a deep blue solution
  3. customThe EtOAc layer was separated
  4. washwashed with brine
  5. customdried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-45817093c08f4bceb010132d064dbc86
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367671B2

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