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

HRID 2298940

반응식

HRID 2298940 반응식
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]

참가 물질

5

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온도
0 °C

실험 절차

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-indole4-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 CH2C12. The combined organic layers were dried (MgSO4) then concentrated in vacuo leaving an orange 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) 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.

후처리

  1. customthen quenched by addition of 5 mL 2 M NaOAc(aq)
  2. customThe layers were separated
  3. extractionthe aqueous layer extracted once with CH2C12
  4. dry with materialThe combined organic layers were dried (MgSO4)
  5. concentrationthen concentrated in vacuo
  6. customleaving an orange oil which
  7. customcrystallized
  8. washThe crystals were rinsed with CH2Cl2
  9. customthen dried in vacuo

출처 및 근거

ORD 기록
ord-663a47f6a4224e27b1cc5caaeaadfe19
출처 데이터셋
uspto-grants-2002_12
특허 번호
US06495541B1

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