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Nitrogen → (1H-Pyrrolo[2,3-b]pyridin-2-yl)methanamine

HRID 1890533
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HRID 1890533 반응식
[NH:1]1[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[C:2]1[C:10]([NH2:12])=O.N#N.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[NH:1]1[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[C:2]1[CH2:10][NH2:12]
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참가 물질

5

반응물 3

HCID 947NitrogenHCID 21226445Aluminium lithium hydrideHCID 446081041H-Pyrrolo[2,3-b]pyridine-2-carboxamide

생성물 1

HCID 67305381(1H-Pyrrolo[2,3-b]pyridin-2-yl)methanamine수율 97.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
80 °C

실험 절차

To a solution of 1H-pyrrolo[2,3-b]pyridine-2-carboxamide (H-2) (805 mg, 5.0 mmol) in dried THF (10 mL) at 0° C. under 1 atm of N2 was slowly added LiAlH4 (570 mg, 15 mmol). The mixture was stirred at 80° C. overnight. The mixture was then cooled to 0° C. concentrated, and then purified by chromatography on silica gel to afford the title compound (720 mg). MS (m/z): 148 (M+1)+.

후처리

  1. customat 0° C.
  2. temperatureThe mixture was then cooled to 0° C.
  3. concentrationconcentrated
  4. custompurified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-91d2a3ca036643b9a15130922d70ea83
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507487B2

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