Sodium hydride → Ethyl 9-(2,5-dichlorobenzyl)-9H-beta-carboline-3-carboxylate

HRID 992556ノート

反応式

HRID 992556 の反応式
[CH:1]1[C:13]2[NH:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[C:3]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[N:2]=1.[H-].[Na+].[H][H].[Cl:23][C:24]1[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:25]=1[CH2:26]Cl>CN(C=O)C.C(O)(=O)C>[Cl:23][C:24]1[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:25]=1[CH2:26][N:12]1[C:13]2[CH:1]=[N:2][C:3]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:4][C:5]=2[C:6]2[C:11]1=[CH:10][CH:9]=[CH:8][CH:7]=2

参加物

7

実験手順

A suspension of ethyl 9H-β-carboline-3-carboxylate (2.40 g, 10 mmol) in anhydrous DMF (20 mL) was cooled in an ice bath under nitrogen. Sodium hydride (420 mg of 60% NaH in mineral oil, 10.5 mmol) was added at once, and the mixture stirred until most of the solids dissolved and hydrogen evolution stopped (approx 10 min). The cool mixture was treated with 2,5-dichlorobenzyl chloride (2.15 g, 1.0 mmol) slowly with stirring, then allowed to warm to room temperature over two hours. The resulting cloudy solution was neutralized with acetic acid, then the solvent was removed in vacuo, affording a tan solid (3.94 g). The crude material was chromatographed on silica gel using a mixture of chloroform and ethyl acetate, affording the title product (1.96 g, 49%). 1H NMR (300 MHz, DMSO-d6) δ9.06 (s, 1 H), 8.96 (s, 1H), 8.48 (d, J=8.0, 1H), 7.55-7.64 (m, 3H), 7.35-7.42 (m, 2H), 6.60 (d,J=2.3, 1H), 5.89 (s, 2H), 4.36 (q, J=6.9, 1H), 1.35 (t, J=7.2, 3H); LRMS calcd for C21H16Cl2N2O2 (M+H) 399, found 399.0.

後処理

  1. temperaturewas cooled in an ice bath under nitrogen
  2. dissolutiondissolved
  3. custom(approx 10 min)
  4. stirringwith stirring
  5. customthe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-9624ccf8e94a4d159e8bfe85c8c8992f
出典データセット
uspto-grants-2002_10
特許番号
US06469021B1

反応ノート

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