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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
ノート
印刷プレビュー

反応式

HRID 2205934 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
25 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-0f603bcfecbe446b955e6a6be3d6b7cd
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09371319B2

反応ノート

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