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Methyl iodide → 5-(2-bromo-4-chloro-6-fluoro-phenyl)-1-methyl-1H-tetrazole

HRID 2046570
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HRID 2046570 반응식
[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([F:9])[C:3]=1[C:10]1[N:11]=[N:12][NH:13][N:14]=1.[C:15]([O-])([O-])=O.[K+].[K+].IC>CN(C=O)C>[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([F:9])[C:3]=1[C:10]1[N:14]([CH3:15])[N:13]=[N:12][N:11]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 679792895-(2-Bromo-4-chloro-6-fluoro-phenyl)-2H-tetrazole

생성물 1

HCID 679793335-(2-bromo-4-chloro-6-fluoro-phenyl)-1-methyl-1H-tetrazole수율 35%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
25 °C

실험 절차

A mixture of 5-(2-bromo-4-chloro-6-fluoro-phenyl)-2H-tetrazole (4.15 g, 14.95 mmol), K2CO3 (3.1 g, 22.43 mmol) and iodomethane (1.3 ml, 20.94 mmol) in DMF (30 ml) was stirred at 25° C. for 3 h. The mixture was partitioned between EtOAc (80 ml) and water (60 ml), the organic layer was separated, washed with water and brine, dried with Na2SO4 and concentrated. The remaining residue was purified by chromatography (silica gel; hexane/EtOAc 100:0-90:10) to obtain 5-(2-bromo-4-chloro-6-fluoro-phenyl)-1-methyl-1H-tetrazole as pale yellow solid (1.5 g, 35%) and the title compound (1.7 g, 39%) as reddish liquid. MS: 291.0 (MH+, 1Br).

후처리

  1. customThe mixture was partitioned between EtOAc (80 ml) and water (60 ml)
  2. customthe organic layer was separated
  3. washwashed with water and brine
  4. dry with materialdried with Na2SO4
  5. concentrationconcentrated
  6. customThe remaining residue was purified by chromatography (silica gel; hexane/EtOAc 100:0-90:10)

출처 및 근거

ORD 기록
ord-aa0513ef51d543ea9292dfee5c4a2f88
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08592426B2

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