Sodium hydride → [3-(3-Nitro-pyrazol-1-ylmethyl)-phenyl]-carbamic acid tert-butyl ester

HRID 546094

反応式

HRID 546094 の反応式
[N+:1]([C:4]1[CH:8]=[CH:7][NH:6][N:5]=1)([O-:3])=[O:2].[H-].[Na+].[C:11]([O:15][C:16](=[O:26])[NH:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH2:24]Br)[CH:19]=1)([CH3:14])([CH3:13])[CH3:12]>CN(C)C=O.C(OCC)(=O)C>[C:11]([O:15][C:16](=[O:26])[NH:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH2:24][N:6]2[CH:7]=[CH:8][C:4]([N+:1]([O-:3])=[O:2])=[N:5]2)[CH:19]=1)([CH3:14])([CH3:13])[CH3:12]

参加物

6

反応物 3

HCID 24758Sodium hydrideHCID 14523558tert-Butyl 3-(bromomethyl)phenylcarbamateHCID 178526745HCID 178526745、化合物

生成物 1

HCID 67194378[3-(3-Nitro-pyrazol-1-ylmethyl)-phenyl]-carbamic acid tert-butyl ester収率 47%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
0 °C

実験手順

3-Nitro-1H-pyrazole (prepared in example 3, 595 mg, 5.26 mmol) was dissolved in anhydrous N,N-dimethylformamide (10 mL) and a 60% dispersion of sodium hydride in mineral oil (211 mg, 5.28 mmol) was added while stirring under nitrogen. After the effervescence ceased and the reaction stirred for an additional 25 min, the reaction was chilled to 0° C. and (3-bromomethyl-phenyl)-carbamic acid tert-butyl ester (1.50 g, 5.26 mmol) was added. The reaction continued to stir under nitrogen at 0° C. for 20 min. The reaction was diluted with ethyl acetate (200 mL), washed with water (2×50 mL), saturated aqueous brine solution (2×20 mL), dried over magnesium sulfate and concentrated in vacuo to give a yellow oil. Purification by flash column (Merck silica gel 60, 40-63 μm; 15% ethyl acetate/hexanes) followed by recrystallization from methylene chloride afforded [3-(3-nitro-pyrazol-1-ylmethyl)-phenyl]-carbamic acid tert-butyl ester (782 mg, 47%) as a beige solid: H1-NMR (400 MHz, DMSO-d6) δ 1.45 (9H, s), 5.39 (2H, s), 6.88 (1H, d, J=7.6 Hz), 7.06 (1H, d, J=2.4 Hz), 7.22 (1H, t, J=8.0 Hz), 7.35 (1H, d, J=8.0 Hz), 7.40 (1H, s), 8.11 (1H, d, J=2.8 Hz), 9.36 (1H, s).

後処理

  1. stirringthe reaction stirred for an additional 25 min
  2. stirringto stir under nitrogen at 0° C. for 20 min
  3. washwashed with water (2×50 mL), saturated aqueous brine solution (2×20 mL)
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customto give a yellow oil
  7. customPurification by flash column (Merck silica gel 60, 40-63 μm; 15% ethyl acetate/hexanes)
  8. customfollowed by recrystallization from methylene chloride

出典と根拠

ORDレコード
ord-fe46e71163464c3cab459d6066d8711b
出典データセット
uspto-grants-2011_05
特許番号
US07935699B2

関連ノート

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