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Sodium Carbonate → N-(4-((4-aminonaphthalen-1-yloxy)methyl)pyridin-2-yl)-2-methoxy acetamide

HRID 2069068
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HRID 2069068 반응식
[CH3:1][O:2][CH2:3][C:4]([NH:6][C:7]1[CH:12]=[C:11]([CH2:13][O:14][C:15]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:18]([N+:25]([O-])=O)=[CH:17][CH:16]=2)[CH:10]=[CH:9][N:8]=1)=[O:5].C(=O)([O-])[O-].[Na+].[Na+]>CC(O)=O.[Fe]>[NH2:25][C:18]1[C:19]2[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:15]([O:14][CH2:13][C:11]2[CH:10]=[CH:9][N:8]=[C:7]([NH:6][C:4](=[O:5])[CH2:3][O:2][CH3:1])[CH:12]=2)=[CH:16][CH:17]=1
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참가 물질

5

반응물 2

HCID 10340Sodium CarbonateHCID 584979032-Methoxy-N-(4-((4-nitronaphthalen-1-yloxy)methyl)pyridin-2-yl)acetamide

생성물 1

HCID 45256716N-(4-((4-aminonaphthalen-1-yloxy)methyl)pyridin-2-yl)-2-methoxy acetamide수율 90.4%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

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온도
50 °C

실험 절차

A suspension of the nitroarene (63) (30.0 g, 82.0 mmol) and iron powder (22.8 g, 408 mmol) in AcOH (300 mL) was heated at 50° C. for 1.5 hr, and was then cooled to RT. Solid sodium carbonate was added portionwise to the reaction mixture until effervescence was no longer observed. The mixture was extracted with ethyl acetate (2×700 mL) and the combined organic extracts were washed with saturated aqueous sodium carbonate and with brine and then dried (MgSO4). Evaporation in vacuo furnished the title compound (Intermediate M) as a brown solid (25.0 g, 77%): m/z 338 (M+H)+ (ES+).

후처리

  1. temperaturewas then cooled to RT
  2. extractionThe mixture was extracted with ethyl acetate (2×700 mL)
  3. washthe combined organic extracts were washed with saturated aqueous sodium carbonate and with brine
  4. dry with materialdried (MgSO4)
  5. customEvaporation in vacuo

출처 및 근거

ORD 기록
ord-07553471f0b4456184334ccfff84133a
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299073B2

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