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4-(5-(3,6-Dihydro-2H-pyran-4-YL)pyrimidin-4-yloxy)aniline → 4-(5-(Tetrahydro-2H-pyran-4-YL)pyrimidin-4-yloxy)aniline

HRID 1880186
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HRID 1880186 반응식
[O:1]1[CH2:6][CH:5]=[C:4]([C:7]2[C:8]([O:13][C:14]3[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=3)=[N:9][CH:10]=[N:11][CH:12]=2)[CH2:3][CH2:2]1>[Pd].[OH-].[Pd+2].[OH-].C(O)C>[O:1]1[CH2:2][CH2:3][CH:4]([C:7]2[C:8]([O:13][C:14]3[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=3)=[N:9][CH:10]=[N:11][CH:12]=2)[CH2:5][CH2:6]1
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참가 물질

5

반응물 1

HCID 593269884-(5-(3,6-Dihydro-2H-pyran-4-YL)pyrimidin-4-yloxy)aniline

생성물 1

HCID 593268884-(5-(Tetrahydro-2H-pyran-4-YL)pyrimidin-4-yloxy)aniline

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 9942167Palladium hydroxide촉매HCID 702Ethanol용매

반응 조건

온도
50 °C

실험 절차

To a pressure vessel was added palladium hydroxide, palladium on carbon (396 mg, 2.82 mmol), ethanol (18.800 ml), and 4-(5-(3,6-dihydro-2H-pyran-4-yl)pyrimidin-4-yloxy)aniline (760 mg, 2.82 mmol). The vessel was purged of air and backfilled with hydrogen (45 psi) before heating to 50° C. for 60 h. It was cooled to room temperature, filtered through Celite, and concentrated under reduced pressure to afford the product as a dark yellow oil. MS (ESI, pos. ion) m/z: 272.1 (M+1).

후처리

  1. customThe vessel was purged of air
  2. temperatureIt was cooled to room temperature
  3. filtrationfiltered through Celite
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-8e2e243520a240ae94f85ffe34cdc087
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318718B2

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