Dimethylformamide → HCID 68550962、化合物

HRID 2382082ノート

反応式

HRID 2382082 の反応式
[CH2:1]([C:3]1[C:11]2[C:6](=[N:7][CH:8]=[CH:9][CH:10]=2)[NH:5][CH:4]=1)[CH3:2].CC([O-])(C)C.[K+].C[N:19](C=O)C>>[CH2:1]([C:3]1[C:11]2[C:6](=[N:7][CH:8]=[CH:9][CH:10]=2)[N:5]([NH2:19])[CH:4]=1)[CH3:2]

参加物

4

実験手順

3-Ethyl-1H-pyrrolo[2,3-b]pyridine (0.91 g, 6.2 mmol) and KOtBu (1.39 g, 12.4 mmol) are dissolved in DMF (28 mL) and stirred for 2 h at rt. While vigorously sparging with nitrogen, NH2Cl (92 ml 0.15 M in ether) is added in portions. The reaction mixture is stirred at rt for 2 h. The mixture is cooled 0° C. and then quenched with Na2S2O3 (2.7 g) in water (50 mL). After standing at rt for 18 h, the mixture is concentrated, triturated in DCM and filtered. The filtrate is concentrated and chromatographed through silica gel eluting with 10% MeOH in DCM to afford 3-ethyl-pyrrolo[2,3-b]pyridin-1-yl-amine (380 mg). MS: 162 (M+H); 1H NMR (300 MHz, CDCl3): δ 8.32 (d, 1H), 7.90 (d, 1H), 7.04-7.13(m, 2H), 4.96 (broad s, 2H), 2.76 (q, 2H), 1.33 (t, 3H).

後処理

  1. customWhile vigorously sparging with nitrogen, NH2Cl (92 ml 0.15 M in ether)
  2. additionis added in portions
  3. stirringThe reaction mixture is stirred at rt for 2 h
  4. temperatureThe mixture is cooled 0° C.
  5. customquenched with Na2S2O3 (2.7 g) in water (50 mL)
  6. waitAfter standing at rt for 18 h
  7. concentrationthe mixture is concentrated
  8. customtriturated in DCM
  9. filtrationfiltered
  10. concentrationThe filtrate is concentrated
  11. customchromatographed through silica gel eluting with 10% MeOH in DCM

出典と根拠

ORDレコード
ord-e2a6cb5074474789b935c82a1db71162
出典データセット
uspto-grants-2012_09
特許番号
US08258130B2

反応ノート

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