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Borane → 3-Methyl-N2-(4-quinolyl)butane-1,2-diamine

HRID 333052
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HRID 333052 반응식
[CH3:1][CH:2]([CH3:18])[CH:3]([NH:7][C:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]=[CH:10][CH:9]=1)[C:4]([NH2:6])=O.B>C1COCC1>[CH3:1][CH:2]([CH3:18])[CH:3]([NH:7][C:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]=[CH:10][CH:9]=1)[CH2:4][NH2:6]
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참가 물질

4

반응물 2

HCID 6331BoraneHCID 668354133-Methyl-2-(4-quinolylamino)butanamide

생성물 1

HCID 651919333-Methyl-N2-(4-quinolyl)butane-1,2-diamine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

3-Methyl-2-(4-quinolylamino)butanamide (460 mg, 1.9 mmol) was dissolved in anhydrous THF (30 ml) under argon, the mixture was cooled to 0° C. and a 1M solution of borane in anhydrous THF (8 ml, 8 mmol) was added with stirring. Stirring was continued for 1 hour at 0° C., the cooling bath was removed and the mixture was allowed to warm to room temperature overnight with stirring. The mixture was quenched with 1M NaOH and extracted with ethyl acetate. The organic phase was evaporated to dryness under reduced pressure and the residue was purified by column chromatography (pre-packed silica column, gradient of ethyl acetate/methanol containing 1% ammonia). 220 mg was obtained (0.96 mmol, 51%). MS (APCI) m/z=229.8 [M+H]+.

후처리

  1. stirringStirring
  2. customthe cooling bath was removed
  3. temperatureto warm to room temperature overnight
  4. stirringwith stirring
  5. customThe mixture was quenched with 1M NaOH
  6. extractionextracted with ethyl acetate
  7. customThe organic phase was evaporated to dryness under reduced pressure
  8. customthe residue was purified by column chromatography (pre-packed silica column, gradient of ethyl acetate/methanol containing 1% ammonia)
  9. custom220 mg was obtained (0.96 mmol, 51%)

출처 및 근거

ORD 기록
ord-0d1befbb89b84c088279b5edcb6197f7
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08877934B2

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