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2,3-Dihydro-1H-indole-2-carboxamide → 2-Aminomethylindoline

HRID 1601076
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HRID 1601076 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[NH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:9][CH:8]1[C:16]([NH2:18])=O>C1COCC1>[NH2:18][CH2:16][CH:8]1[CH2:9][C:10]2[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=2)[NH:7]1
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참가 물질

4

반응물 2

HCID 139378102,3-Dihydro-1H-indole-2-carboxamideHCID 21226445Aluminium lithium hydride2회

생성물 1

HCID 218304062-Aminomethylindoline수율 51%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

LAH (20 mL, 1M solution in THF) was added dropwise through a syringe to a solution of (±)-indoline-2-carboxamide (2.2 g, 13.6 mmol) in anhydrous THF (20 mL) with cooling, and the resulting solution was refluxed under argon for 5 h. More LAH (20 mL) was added, and reflux was continued for another 6 h. 10% aqueous THF was added dropwise with cooling to destroy excess LAH, and then Et2O was added. After stirring for 10 min, the colorless precipitate was removed by filtration and washed with THF. The filtrate was dried (K2CO3), concentrated, and purified by silica gel flash chromatography (90:10:0.2 CH2Cl2 /MeOH/Et3N). The title compound (1.02 g, 51%) was obtained as an amber oil: MS (ES) m/e 149.0 (M+H)+.

후처리

  1. temperaturewith cooling
  2. temperaturethe resulting solution was refluxed under argon for 5 h
  3. temperaturereflux
  4. temperaturewith cooling
  5. customto destroy excess LAH
  6. additionEt2O was added
  7. customthe colorless precipitate was removed by filtration
  8. washwashed with THF
  9. dry with materialThe filtrate was dried (K2CO3)
  10. concentrationconcentrated
  11. custompurified by silica gel flash chromatography (90:10:0.2 CH2Cl2 /MeOH/Et3N)

출처 및 근거

ORD 기록
ord-1f0214d779e84795af0f569e1d3eee14
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05977101

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