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6-Bromo-2-(diethoxymethyl)-1H-pyrrolo[3,2-c]pyridine → 6-Bromo-1H-pyrrolo[3,2-c]pyridine-2-carbaldehyde

HRID 2205934
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HRID 2205934 반응식
[Br:1][C:2]1[N:7]=[CH:6][C:5]2[CH:8]=[C:9]([CH:11](OCC)[O:12]CC)[NH:10][C:4]=2[CH:3]=1>C1COCC1.O>[Br:1][C:2]1[N:7]=[CH:6][C:5]2[CH:8]=[C:9]([CH:11]=[O:12])[NH:10][C:4]=2[CH:3]=1
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참가 물질

4

반응물 1

HCID 867063196-Bromo-2-(diethoxymethyl)-1H-pyrrolo[3,2-c]pyridine

생성물 1

HCID 867063216-Bromo-1H-pyrrolo[3,2-c]pyridine-2-carbaldehyde수율 105.9%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

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온도
25 °C

실험 절차

To a solution of 6-Bromo-2-(diethoxymethyl)-1H-pyrrolo[3,2-c]pyridine (Preparation 137, 142 mg, 0.47 mmole) in THF (1.4 mL) and water (0.28 mL) was added tosic acid hydrate (134 mg, 0.705 mmole) and the reaction was stirred at 25° C. for 55 minutes. The reaction was partitioned between ethyl acetate (20 mL) and sodium bicarbonate (5 mL). The layers were separated and the aqueous layer again extracted with ethyl acetate (7 mL). The combined organic layers were washed with sodium bicarbonate and brine and concentrated in vacuo to afford the title compound (112 mg). 1H-NMR (CDCl3, 500 MHz): δ 7.37 (s, 1H), 7.62 (t, J=0.95 Hz, 1H), 8.88 (d, J=0.95 Hz, 1H), 9.32 (br s, 1H), 9.93 (s, 1H).

후처리

  1. customThe reaction was partitioned between ethyl acetate (20 mL) and sodium bicarbonate (5 mL)
  2. customThe layers were separated
  3. extractionthe aqueous layer again extracted with ethyl acetate (7 mL)
  4. washThe combined organic layers were washed with sodium bicarbonate and brine
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0f603bcfecbe446b955e6a6be3d6b7cd
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09371319B2

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