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Potassium Carbonate → Tert-butyl 4-(2-methyl-4-nitrophenoxy)pyridin-2-ylcarbamate

HRID 240552
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HRID 240552 반응식
[OH:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH:8][C:9](=[O:15])[O:10][C:11]([CH3:14])([CH3:13])[CH3:12])[CH:3]=1.F[C:17]1[CH:22]=[CH:21][C:20]([N+:23]([O-:25])=[O:24])=[CH:19][C:18]=1[CH3:26].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH3:26][C:18]1[CH:19]=[C:20]([N+:23]([O-:25])=[O:24])[CH:21]=[CH:22][C:17]=1[O:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH:8][C:9](=[O:15])[O:10][C:11]([CH3:12])([CH3:14])[CH3:13])[CH:3]=1
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 68001Benzene, 1-fluoro-2-methyl-4-nitro-HCID 178452896HCID 178452896, 화합물

생성물 1

HCID 66937340Tert-butyl 4-(2-methyl-4-nitrophenoxy)pyridin-2-ylcarbamate수율 30%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
65 °C

실험 절차

To a solution of tert-butyl 4-hydroxypyridin-2-ylcarbamate (4.12 g, 19.6 mmol) and 1-fluoro-2-methyl-4-nitrobenzene (3.34 g, 21.6 mmol) in DMF (40 mL) was added K2CO3 (4.06 g, 29.04 mmol). After heating to 65° C. for 64 hours, the mixture was cooled to room temperature and poured into ice water (200 mL). The reaction mixture was extracted several times with ethyl acetate. The combined organics were concentrated under reduced pressure. The residue was chromatographed (20% ethyl acetate in hexanes) to provide the product (2.03 g, 30%).

후처리

  1. temperaturethe mixture was cooled to room temperature
  2. extractionThe reaction mixture was extracted several times with ethyl acetate
  3. concentrationThe combined organics were concentrated under reduced pressure
  4. customThe residue was chromatographed (20% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-78620a617fd748c29ce9748025b19eeb
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08648087B2

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