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Aluminium lithium hydride → 4-[2-(3-Methyl-butylamino)-thiazol-4-yl]-benzylamine

HRID 1191071
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HRID 1191071 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][CH:8]([CH3:25])[CH2:9][CH2:10][NH:11][C:12]1[S:13][CH:14]=[C:15]([C:17]2[CH:24]=[CH:23][C:20]([C:21]#[N:22])=[CH:19][CH:18]=2)[N:16]=1>C1COCC1>[CH3:7][CH:8]([CH3:25])[CH2:9][CH2:10][NH:11][C:12]1[S:13][CH:14]=[C:15]([C:17]2[CH:18]=[CH:19][C:20]([CH2:21][NH2:22])=[CH:23][CH:24]=2)[N:16]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 244317014-[2-(3-Methyl-butylamino)-thiazol-4-yl]-benzonitrile

생성물 1

HCID 598288274-[2-(3-Methyl-butylamino)-thiazol-4-yl]-benzylamine수율 99.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
60 °C

실험 절차

Add lithium aluminum hydride (210 mg, 5.5 mmol) portionwise over 3 min to a solution of 4-[2-(3-methyl-butylamino)-thiazol-4-yl]-benzonitrile (500 mg, 1.8 mmol) in THF (20 mL) at room temperature under a nitrogen atmosphere. Stir the mixture for 1 h at 60° C. Cool the mixture, quench slowly with water (0.2 mL) and 1N NaOH (0.2 mL). Add sodium sulfate to absorb residual water, filter the mixture through Celite®, wash with DCM (50 mL) and concentrate in vacuo. Purify the residue by SCX chromatography to obtain the desired intermediate (493 mg, 97%). MS (ES+) m/z: 276 (M+H)+.

후처리

  1. temperatureCool the mixture
  2. customquench slowly with water (0.2 mL) and 1N NaOH (0.2 mL)
  3. customAdd sodium sulfate to absorb residual water
  4. filtrationfilter the mixture through Celite®
  5. washwash with DCM (50 mL)
  6. concentrationconcentrate in vacuo
  7. customPurify the residue by SCX chromatography

출처 및 근거

ORD 기록
ord-9f1741e1679c403ca6f0d4a053bfff13
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680091B2

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