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Acetic Acid → 6-Bromo-2-methoxy-3-methyl-3h-imidazo[4,5-b]pyridine

HRID 445626
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HRID 445626 반응식
[Br:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([NH:8][CH3:9])=[N:6][CH:7]=1.[CH3:11][O:12][C:13](OC)(OC)OC.C(O)(=O)C>CCOC(C)=O>[Br:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:13]([O:12][CH3:11])[N:8]([CH3:9])[C:5]2=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 74613Tetramethyl orthocarbonateHCID 151940325-Bromo-N2-methylpyridine-2,3-diamine

생성물 1

HCID 104668936-Bromo-2-methoxy-3-methyl-3h-imidazo[4,5-b]pyridine

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

A solution of 5-bromo-N*2*-methyl-pyridine-2,3-diamine (Stage 67.1.4, 960 mg, 4.75 mmol) and tetramethylorthocarbonate (Aldrich, Buchs, Switzerland, 2 ml, 14.7 mmol) and acetic acid (0.273 ml, 4.75 mmol) was stirred for 90 min at 100° C. The reaction mixture was diluted with EtOAc and washed with saturated aqueous NaHCO3 and brine. The aqueous layer was extracted with EtOAc and the combined organic layers washed with saturated aqueous NaHCO3 and with brine, then dried over Na2SO4, filtered and evaporated. The crude product was dry loaded on silica gel and purified by MPLC (DCM/MeOH 0%-4%) to give the title compound as a green solid. (HPLC: tR 2.83 min (Method A); M+H=242, 244 MS-ES).

후처리

  1. washwashed with saturated aqueous NaHCO3 and brine
  2. extractionThe aqueous layer was extracted with EtOAc
  3. washthe combined organic layers washed with saturated aqueous NaHCO3 and with brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. customevaporated
  7. dry with materialThe crude product was dry
  8. custompurified by MPLC (DCM/MeOH 0%-4%)

출처 및 근거

ORD 기록
ord-762eb65f4ecb497c83757d2cdc28c6bc
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08476294B2

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