Hydrochloric Acid → ethyl 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylate

HRID 12827

반응식

HRID 12827 반응식
N(OC(C)(C)C)=O.[CH2:8]([O:10][C:11]([C:13]1[CH:14]=[N:15][N:16]([C:19]([CH3:22])([CH3:21])[CH3:20])[C:17]=1N)=[O:12])[CH3:9].[ClH:23]>C(#N)C>[CH2:8]([O:10][C:11]([C:13]1[CH:14]=[N:15][N:16]([C:19]([CH3:22])([CH3:21])[CH3:20])[C:17]=1[Cl:23])=[O:12])[CH3:9]

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 10906Tert-Butyl nitriteHCID 13809946ethyl 5-amino-1-(tert-butyl)-1H-pyrazole-4-carboxylate

생성물 1

HCID 13809947ethyl 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylate수율 39%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a mixture of t-butyl nitrite (7.2 mL, 60.5 mmol), cuprous chloride (4.8 g, 48.5 mmol), and anhydrous acetonitrile (120 mL) was added 5-amino-1-tert-butyl-1H-pyrazole-4-carboxylic acid ethyl ester (8.4 g, 39.8 mmol) in portions over 30 minutes at 0° C. The reaction mixture was stirred at room temperature for 1 h, then at 65° C. for 1 h. The mixture was then poured into 6N HCl (120 mL) and extracted with dichloromethane. The aqueous phase was extracted three times with dichloromethane. After the combined organic phases were concentrated in vacuo, the crude residue was purified by flash chromatography eluting with a gradient of 0-20% ethyl acetate/hexanes, then 20% ethyl acetate/hexanes to give 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid ethyl ester (5.5 g, 39%).

후처리

  1. waitat 65° C. for 1 h
  2. extractionextracted with dichloromethane
  3. extractionThe aqueous phase was extracted three times with dichloromethane
  4. concentrationAfter the combined organic phases were concentrated in vacuo
  5. customthe crude residue was purified by flash chromatography
  6. washeluting with a gradient of 0-20% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-04c1057d28d84cdc850db8b6d209f025
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07728029B2

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