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Potassium Carbonate → 2-(Imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehyde

HRID 1473887
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HRID 1473887 반응식
Cl[CH2:2][C:3]1[C:4]2[N:5]([CH:9]=[CH:10][N:11]=2)[CH:6]=[CH:7][CH:8]=1.[OH:12][C:13]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:14]=1[CH:15]=[O:16].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[N:11]1[CH:10]=[CH:9][N:5]2[CH:6]=[CH:7][CH:8]=[C:3]([CH2:2][O:12][C:13]3[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:14]=3[CH:15]=[O:16])[C:4]=12
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 956952-Hydroxy-5-methoxybenzaldehydeHCID 216615828-(Chloromethyl)imidazo[1,2-a]pyridine

생성물 1

HCID 716214602-(Imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehyde수율 45%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
87.5 °C

실험 절차

To a solution of the crude 8-(chloromethyl)imidazo[1,2-a]pyridine (6.8 mmol, 1 eq) and 2-hydroxy-5-methoxybenzaldehyde (1.3 g, 8.1 mmol, 1.2 eq) in DMF (20 mL) was added potassium carbonate (2.8 g, 20.4 mmol, 3 eq) and the reaction mixture was heated at 85-90° C. for 5 h. DMF was removed under vacuum and the residue was taken in ethyl acetate and filtered. The solid was washed with additional ethyl acetate, and then dried and evaporated to give the crude, which was purified by column chromatography (EtOAc/Hexane) to yield the desired compound in 45% yield. NMR (400 MHz, CDCl3): δ 3.80 (s, 3H), 5.60 (s, 2H), 6.85 (d, 1H), 7.12 (d, 2H), 7.36 (m, 2H), 7.66 (m, 2H), 8.14 (m, 1H), 10.58 (s, 1H); MS: exact mass calculated for C16H14N2O3, 282.10; m/z found, 283 [M+H]+.

후처리

  1. customDMF was removed under vacuum
  2. filtrationfiltered
  3. washThe solid was washed with additional ethyl acetate
  4. customdried
  5. customevaporated
  6. customto give the crude, which
  7. customwas purified by column chromatography (EtOAc/Hexane)

출처 및 근거

ORD 기록
ord-0eb5b9b6080743bdb70dd0e756544964
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09018210B2

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