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N-bromobutanimide → Methyl 4-(3-amino-6-bromopyrazin-2-yl)-2-fluorobenzoate

HRID 595989
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HRID 595989 반응식
[NH2:1][C:2]1[C:3]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[C:10]([F:18])[CH:9]=2)=[N:4][CH:5]=[CH:6][N:7]=1.C1C(=O)N([Br:26])C(=O)C1.C(=O)(O)[O-].[Na+]>C(#N)C>[NH2:1][C:2]1[C:3]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[C:10]([F:18])[CH:9]=2)=[N:4][C:5]([Br:26])=[CH:6][N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 67184N-bromobutanimideHCID 516892Sodium BicarbonateHCID 118045820Methyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoate

생성물 1

HCID 118046172Methyl 4-(3-amino-6-bromopyrazin-2-yl)-2-fluorobenzoate수율 96%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a suspension of methyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoate (31.5 g, 127 mmol) in acetonitrile (430 mL) at 0° C. was added NBS (23.9 g, 134 mmol). The reaction mixture was stirred in ice bath for 1 h, sat. sodium bicarbonate was added, stirred 30 min and product was extracted with ethylacetate. The organic extracts were combined, washed with brine, dried over sodium sulfate, filtered and evaporated. The crude product was recrystallized in EtOAc and heptane to give methyl 4-(3-amino-6-bromopyrazin-2-yl)-2-fluorobenzoate as brown color solid in 96% yield. LCMS (m/z): 326.0/328.0 (MH+), 0.87 min.

후처리

  1. stirringstirred 30 min
  2. extractionproduct was extracted with ethylacetate
  3. washwashed with brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude product was recrystallized in EtOAc

출처 및 근거

ORD 기록
ord-6cc97469cd2f4be0bc9977d100da46bb
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242996B2

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