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Aluminium lithium hydride → HCID 67335147, 화합물

HRID 1672157
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HRID 1672157 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([NH:10][C:11]3([C:17]#[N:18])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]3)=[CH:7][CH:8]=2)[CH:3]=[N:2]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[NH2:18][CH2:17][C:11]1([NH:10][C:6]2[CH:5]=[C:4]3[C:9](=[CH:8][CH:7]=2)[NH:1][N:2]=[CH:3]3)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 67336325HCID 67336325, 화합물

생성물 1

HCID 67335147HCID 67335147, 화합물수율 31%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
70 °C

실험 절차

To a stirred solution of 1-(1H-indazol-5-ylamino)-cyclohexanecarbonitrile (2.53 g, 10.5 mmol) in THF (40 mL) at room temperature and under nitrogen was added LiAlH4 (21.0 mL of a 1.0 M solution in THF, 21.0 mmol) dropwise over 3 minutes. After 30 minutes the reaction mixture was warmed to 70° C. After 2 hours the reaction mixture was cooled and stirred at ambient temperature for 14 hours, then quenched by the addition of sodium sulfate decahydrate (3 g). The reaction mixture was diluted with DCM:MeOH:NH4OH (90:9:1, 200 mL) then filtered and concentrated in vacuo. Purification by chromatography (silica, 3 to 20% of a 9:1 MeOH:NH4OH solution in DCM) gave (1-aminomethyl-cyclohexyl)-(1H-indazol-5-yl)-amine (0.785 g, 3.22 mmol, 31 %) as a solid.

후처리

  1. temperatureAfter 2 hours the reaction mixture was cooled
  2. customquenched by the addition of sodium sulfate decahydrate (3 g)
  3. additionThe reaction mixture was diluted with DCM:MeOH:NH4OH (90:9:1, 200 mL)
  4. filtrationthen filtered
  5. concentrationconcentrated in vacuo
  6. customPurification by chromatography (silica, 3 to 20% of a 9:1 MeOH:NH4OH solution in DCM)

출처 및 근거

ORD 기록
ord-9a08f65eeb664d419e1cf3a00c399db4
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07998963B2

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