Dimethylformamide → 2-(4-chloro-phenyl)-3-formyl-1H-indole-4-carboxylic acid methyl ester

HRID 489559

反応式

HRID 489559 の反応式
P(Cl)(Cl)(Cl)=O.CN([CH:9]=[O:10])C.[CH3:11][O:12][C:13]([C:15]1[C:16]2[CH:17]=[C:18]([C:24]3[CH:29]=[CH:28][C:27]([Cl:30])=[CH:26][CH:25]=3)[NH:19][C:20]=2[CH:21]=[CH:22][CH:23]=1)=[O:14]>C(Cl)Cl>[CH3:11][O:12][C:13]([C:15]1[C:16]2[C:17]([CH:9]=[O:10])=[C:18]([C:24]3[CH:29]=[CH:28][C:27]([Cl:30])=[CH:26][CH:25]=3)[NH:19][C:20]=2[CH:21]=[CH:22][CH:23]=1)=[O:14]

参加物

5

反応条件

温度
0 °C

実験手順

Phosphorous oxychloride (0.42 g, 2.71 mmol) was added to DMF (0.99 g, 13.57 mmol) at 0° C. The resulting colorless solution was added dropwise to a solution of 2-(4-chloro-phenyl)-1H-indole-4-carboxylic acid methyl ester (0.52 g, 1.81 mmol) in 10 mL dry CH2Cl2 at 0° C. The reaction was stirred at 0° C. for 10 min then quenched by addition of 5 mL 2 M NaOAc(aq). The layers were separated and the aqueous layer extracted once with CH2Cl2. The combined organic layers were dried (MgSO4) then concentrated in vacuo leaving anorange oil which crystallized on standing. The crystals were rinsed with CH2Cl2 then dried in vacuo to yield 2-(4-chloro-phenyl)-3-formyl-1H-indole-4-carboxylic acid methyl ester, 231 mg (41%) as an off-white solid: m.p. 221-222° C.; 1H NMR (300 MHz, d6-DMSO) δ 3.93 (s, 3H), 7.49 (app t, J=7.5 Hz, 1H), 7.71 (m, 4H), 7.94 (d, J=7.8 Hz, 2H), 9.71 (s, 1H), 13.67 (br s, 1H). MS (electrospray, [M−H]) 312.

後処理

  1. customthen quenched by addition of 5 mL 2 M NaOAc(aq)
  2. customThe layers were separated
  3. extractionthe aqueous layer extracted once with CH2Cl2
  4. dry with materialThe combined organic layers were dried (MgSO4)
  5. concentrationthen concentrated in vacuo
  6. customleaving anorange oil which
  7. customcrystallized
  8. washThe crystals were rinsed with CH2Cl2
  9. customthen dried in vacuo

出典と根拠

ORDレコード
ord-e3a528d2883440eb812242968eb86dfa
出典データセット
uspto-grants-2005_12
特許番号
US06977298B2

関連ノート

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