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Sodium Hydroxide → HCID 86722462, 화합물

HRID 718848
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HRID 718848 반응식
[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][C:10]([F:13])=[CH:9][CH:8]=2)[N:5]=[CH:4][C:3]=1[C:14]#N.[H][H].[OH-:18].[Na+]>[Ni].O.C(O)(=O)C>[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][C:10]([F:13])=[CH:9][CH:8]=2)[N:5]=[CH:4][C:3]=1[CH:14]=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 14798Sodium HydroxideHCID 6886855-amino-1-(4-fluorophenyl)-1H-pyrazole-4-carbonitrileHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 86722462HCID 86722462, 화합물

시약·촉매·용매 3

HCID 935Nickel촉매HCID 176Acetic Acid용매
HCID 962
Water
용매
3회

실험 절차

5-Amino-1-(4-fluorophenyl)-1H-pyrazole-4-carbonitrile (110, R1=4-Fluorophenyl) (56.2 g, 278 mmol), acetic acid (270 mL), water (75 mL) and Raney 2400 Nickel slurry in water (15 g, 278 mmol) was shaken under about 30 psi hydrogen at about 20°-25° C. for about 8 h. The mixture was filtered through a pad of Celite®. The contents of the reaction vessel were transferred with acetic acid (150 mL) and the pad was washed with an additional portion of acetic acid (200 mL). The filtrate was concentrated under reduced pressure to give a slurry. Water (300 mL) was added then the mixture was stirred for about 15 min. The mixture was cooled in an ice/water bath then basified with 5 N aq. NaOH. After stirring for about 20 min in the ice/water bath the solids were collected by filtration and washed with water (100 mL).

후처리

  1. filtrationThe mixture was filtered through a pad of Celite®
  2. washthe pad was washed with an additional portion of acetic acid (200 mL)
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. customto give a slurry
  5. temperatureThe mixture was cooled in an ice/water bath
  6. filtrationwere collected by filtration
  7. washwashed with water (100 mL)

출처 및 근거

ORD 기록
ord-cd85ba35108747639e0526606092fb65
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09193744B2

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