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Ammonium formate → HCID 22630777, 화합물

HRID 2416553
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HRID 2416553 반응식
[CH3:1][O:2][CH:3]1[C:7]([C:8]2[CH:13]=[CH:12][C:11]([C:14]3[N:19]=[CH:18][CH:17]=[CH:16][N:15]=3)=[CH:10][CH:9]=2)=[CH:6][CH:5]([O:20][CH3:21])[O:4]1.C([O-])=O.[NH4+]>CO.[Pd]>[CH3:1][O:2][CH:3]1[CH:7]([C:8]2[CH:13]=[CH:12][C:11]([C:14]3[N:15]=[CH:16][CH:17]=[CH:18][N:19]=3)=[CH:10][CH:9]=2)[CH2:6][CH:5]([O:20][CH3:21])[O:4]1
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참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 22631085HCID 22631085, 화합물

생성물 1

HCID 22630777HCID 22630777, 화합물수율 85%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A mixture of 2,5-dihydro-2,5-dimethoxy-3-[4-(pyrimidin-2-yl)phenyl]furan (70 mg, 0.25 mmol), 10% Pd/C (20 mg), and ammonium formate (46 mg, 0.75 mmol) in methanol (1 mL) was stirred overnight. The reaction mixture was filtered through a fritted funnel, and concentrated in vacuo. The crude product was partitioned between ethyl acetate and sat. aq. NaHCO3, the organic layer dried with Na2SO4, and concentrated in vacuo to give 60 mg (85%) of the title compound, which was used without further purification. MS 287 (M+H)+.

후처리

  1. filtrationThe reaction mixture was filtered through a fritted funnel
  2. concentrationconcentrated in vacuo
  3. customThe crude product was partitioned between ethyl acetate and sat. aq. NaHCO3
  4. dry with materialthe organic layer dried with Na2SO4
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-1ae37e00f33a4bd8ae66a14bc206afee
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06825170B2

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