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tert-butyl (3R)-3-{benzyl[(1R)-1-phenylethyl]amino}heptanoate → tert-butyl (3R)-3-aminoheptanoate

HRID 64405
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인쇄 미리보기

반응식

HRID 64405 반응식
C([N:8]([C@@H](C1C=CC=CC=1)C)[C@H:9]([CH2:18][CH2:19][CH2:20][CH3:21])[CH2:10][C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])C1C=CC=CC=1>CO.[C].[Pd]>[NH2:8][C@H:9]([CH2:18][CH2:19][CH2:20][CH3:21])[CH2:10][C:11]([O:13][C:14]([CH3:15])([CH3:16])[CH3:17])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86713413tert-butyl (3R)-3-{benzyl[(1R)-1-phenylethyl]amino}heptanoate

생성물 1

HCID 86713412tert-butyl (3R)-3-aminoheptanoate수율 78.6%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 887Methanol용매

실험 절차

To a solution of 1.15 g of tert-butyl (3R)-3-{benzyl[(1R)-1-phenylethyl]amino}heptanoate in 30 ml of methanol was added 450 mg of 10% palladium-carbon, followed by stirring overnight under a hydrogen atmosphere at 4 atm. The reaction mixture was filtered over Celite and the solvent was then evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 460 mg of tert-butyl (3R)-3-aminoheptanoate.

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후처리

  1. filtrationThe reaction mixture was filtered over Celite
  2. customthe solvent was then evaporated under reduced pressure
  3. customThe obtained residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-d166927b3c2e44feaa18d7ebbda2a906
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09447090B2

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