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(R)-methyl 6-(4-fluoro-3-methylbenzyloxy)-2-azidohexanoate → (R)-methyl 6-(4-fluoro-3-methylbenzyloxy)-2-aminohexanoate

HRID 885516
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HRID 885516 반응식
[F:1][C:2]1[CH:21]=[CH:20][C:5]([CH2:6][O:7][CH2:8][CH2:9][CH2:10][CH2:11][C@@H:12]([N:17]=[N+]=[N-])[C:13]([O:15][CH3:16])=[O:14])=[CH:4][C:3]=1[CH3:22]>C(OCC)(=O)C.[Pd]>[F:1][C:2]1[CH:21]=[CH:20][C:5]([CH2:6][O:7][CH2:8][CH2:9][CH2:10][CH2:11][C@@H:12]([NH2:17])[C:13]([O:15][CH3:16])=[O:14])=[CH:4][C:3]=1[CH3:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86667072(R)-methyl 6-(4-fluoro-3-methylbenzyloxy)-2-azidohexanoate

생성물 1

HCID 69170604(R)-methyl 6-(4-fluoro-3-methylbenzyloxy)-2-aminohexanoate수율 99%

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 23938Palladium용매

실험 절차

To a solution of (R)-methyl 6-(4-fluoro-3-methylbenzyloxy)-2-azidohexanoate (0.141 g, 0.453 mmol) in 10 mL of ethyl acetate, Pd on BaSO4 (0.070 g) was added. The mixture was flushed with H2 for 15 min and stirred at room temperature under H2 for 1 h. The reaction mixture was then filtered through a pad of Celite and washed with ethyl acetate. The filtrate was concentrated under reduced pressure. The residue was used in the next step without further purification (0.128 g, >99% yield). GC-MS: tR=4.0 min; m/z 283 (M+).

후처리

  1. customThe mixture was flushed with H2 for 15 min
  2. filtrationThe reaction mixture was then filtered through a pad of Celite
  3. washwashed with ethyl acetate
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. customThe residue was used in the next step without further purification (0.128 g, >99% yield)

출처 및 근거

ORD 기록
ord-f6d814c72ece45169f70179df0eb62ae
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08242174B2

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