Aniline → 6-(dimethylamino)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide

HRID 645360

반응식

HRID 645360 반응식
C[Al](C)C.[NH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[CH3:12][N:13]([CH3:28])[C:14]1[CH:15]=[CH:16][C:17]2[N:18]([CH:20]=[C:21]([C:23](OCC)=[O:24])[N:22]=2)[CH:19]=1.[Cl-].[NH4+]>C1(C)C=CC=CC=1>[CH3:12][N:13]([CH3:28])[C:14]1[CH:15]=[CH:16][C:17]2[N:18]([CH:20]=[C:21]([C:23]([NH:5][C:6]3[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=3)=[O:24])[N:22]=2)[CH:19]=1

참가 물질

6

반응물 4

HCID 6115AnilineHCID 25517Ammonium ChlorideHCID 16682925TrimethylaluminumHCID 44124134Ethyl 6-dimethylaminoimidazo[1,2-a]pyridine-2-carboxylate

생성물 1

HCID 247716096-(dimethylamino)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

0.46 ml of a 2M solution of trimethylaluminum in toluene is added dropwise to a solution, cooled to 0° C., of 60.8 μl of aniline in 3 ml of toluene, followed, at 20° C., by the addition of 76 mg of ethyl 6-dimethylaminoimidazo[1,2-a]pyridine-2-carboxylate. The reaction mixture is stirred at ambient temperature for 15 minutes. It is cooled to 0° C. and then 20 ml of a saturated ammonium chloride solution are added. The organic phase is dried over magnesium sulfate, filtered through Celite and evaporated to dryness under reduced pressure. The residue is chromatographed on a silica cartridge, elution being carried out with a mixture of dichloromethane and ethyl acetate. The fractions comprising the product are combined and concentrated to dryness under reduced pressure. The residue obtained is crystallized from methanol to give 36 mg of 6-(dimethylamino)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a gray powder.

후처리

  1. temperatureIt is cooled to 0° C.
  2. dry with materialThe organic phase is dried over magnesium sulfate
  3. filtrationfiltered through Celite
  4. customevaporated to dryness under reduced pressure
  5. customThe residue is chromatographed on a silica cartridge, elution
  6. additionbeing carried out with a mixture of dichloromethane and ethyl acetate
  7. concentrationconcentrated to dryness under reduced pressure
  8. customThe residue obtained
  9. customis crystallized from methanol

출처 및 근거

ORD 기록
ord-6d14154c6071465e8168695abf3e2204
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07704989B2

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