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N-{(S)-1-hydroxy-3-phenyl-2-propyl}-5-benzyloxy-2-hydroxybenzamide → N-{(S)-1-hydroxy-3-phenyl-2-propyl}-2,5-dihydroxybenzamide

HRID 1243272
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HRID 1243272 반응식
[OH:1][CH2:2][C@@H:3]([NH:11][C:12](=[O:28])[C:13]1[CH:18]=[C:17]([O:19]CC2C=CC=CC=2)[CH:16]=[CH:15][C:14]=1[OH:27])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1>CO>[OH:1][CH2:2][C@@H:3]([NH:11][C:12](=[O:28])[C:13]1[CH:18]=[C:17]([OH:19])[CH:16]=[CH:15][C:14]=1[OH:27])[CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 17751795N-{(S)-1-hydroxy-3-phenyl-2-propyl}-5-benzyloxy-2-hydroxybenzamide

생성물 1

HCID 10469284N-{(S)-1-hydroxy-3-phenyl-2-propyl}-2,5-dihydroxybenzamide수율 85%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

In a flask equipped with a magnetic stirring bar and a rubber septum is dissolved the N-{(S)-1-hydroxy-3-phenyl-2-propyl}-5-benzyloxy-2-hydroxybenzamide in methanol. Nitrogen is bubbled through the solution and 10% Pd on charcoal is added. After flushing with nitrogen, the suspension is placed under hydrogen atmosphere and stirred for 2 hours. The suspension is flushed with nitrogen and filtered and rinsed over Celite. The filtrate is concentrated under vacuum. In this fashion is obtained N-{(S)-1-hydroxy-3-phenyl-2-propyl}-2,5-dihydroxybenzamide (85%).

후처리

  1. customIn a flask equipped with a magnetic stirring bar
  2. customNitrogen is bubbled through the solution and 10% Pd on charcoal
  3. additionis added
  4. customAfter flushing with nitrogen
  5. customThe suspension is flushed with nitrogen
  6. filtrationfiltered
  7. washrinsed over Celite
  8. concentrationThe filtrate is concentrated under vacuum

출처 및 근거

ORD 기록
ord-c985136e55be464b952aacd30c033b21
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07119068B2

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