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4-(1-tert-Butoxypropan-2-yloxy)-7-methoxyquinoline → 2-(7-Methoxyquinolin-4-yloxy)propan-1-ol

HRID 1878697
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반응식

HRID 1878697 반응식
C([O:5][CH2:6][CH:7]([O:9][C:10]1[C:19]2[C:14](=[CH:15][C:16]([O:20][CH3:21])=[CH:17][CH:18]=2)[N:13]=[CH:12][CH:11]=1)[CH3:8])(C)(C)C>C(O)(C(F)(F)F)=O>[CH3:21][O:20][C:16]1[CH:15]=[C:14]2[C:19]([C:10]([O:9][CH:7]([CH3:8])[CH2:6][OH:5])=[CH:11][CH:12]=[N:13]2)=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 598430204-(1-tert-Butoxypropan-2-yloxy)-7-methoxyquinoline

생성물 1

HCID 688094362-(7-Methoxyquinolin-4-yloxy)propan-1-ol

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of 4-(1-tert-butoxypropan-2-yloxy)-7-methoxyquinoline in TFA (10 mL) was stirred for 45 min at 23° C. The solvent was removed under reduced pressure and the residue was partitioned between CH2Cl2 and 10% Na2CO3. The aqueous layer was extracted with CH2Cl2 (5 mL×4) and the combined organics were dried over MgSO4. The mixture was purified on 12 grams of silica eluting with 0-100% of 5% MeOH/CH2Cl2. MS (ESI pos. ion) m/z (MH+): 234. Calc'd exact mass for C13H15NO3: 233.

후처리

  1. customThe solvent was removed under reduced pressure
  2. custom
the residue was partitioned between CH2Cl2 and 10% Na2CO3
  • extractionThe aqueous layer was extracted with CH2Cl2 (5 mL×4)
  • dry with materialthe combined organics were dried over MgSO4
  • customThe mixture was purified on 12 grams of silica eluting with 0-100% of 5% MeOH/CH2Cl2
  • 출처 및 근거

    ORD 기록
    ord-1574bb056f6043b1b9eaf6ec7fbce1a0
    출처 데이터셋
    uspto-grants-2012_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08314087B2

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