3-Fluorobenzyl isocyanate → 2-(2,3-dihydro-1-benzofuran-5-ylcarbonyl)-N-(3-fluorobenzyl)hydrazinecarboxamide

HRID 452601

反応式

HRID 452601 の反応式
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([NH:12][NH2:13])=[O:11])=[CH:9][C:4]=2[CH2:3][CH2:2]1.[F:14][C:15]1[CH:16]=[C:17]([CH:22]=[CH:23][CH:24]=1)[CH2:18][N:19]=[C:20]=[O:21]>N1C=CC=CC=1.C(OCC)(=O)C>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([NH:12][NH:13][C:20]([NH:19][CH2:18][C:17]3[CH:22]=[CH:23][CH:24]=[C:15]([F:14])[CH:16]=3)=[O:21])=[O:11])=[CH:9][C:4]=2[CH2:3][CH2:2]1

参加物

5

反応物 2

HCID 6434993-Fluorobenzyl isocyanateHCID 185264692,3-Dihydro-1-benzofuran-5-carbohydrazide

生成物 1

HCID 686644512-(2,3-dihydro-1-benzofuran-5-ylcarbonyl)-N-(3-fluorobenzyl)hydrazinecarboxamide収率 65%

試薬・触媒・溶媒 2

HCID 1049Pyridine溶媒HCID 8857Ethyl Acetate溶媒

実験手順

A solution of 2,3-dihydro-1-benzofuran-5-carbohydrazide (0.50 g, 2.81 mmol) and 3-fluorobenzyl isocyanate (0.85 g, 5.61 mmol) in pyridine (5 mL) was stirred at room temperature for 3 days. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was washed with ethyl acetate to give the title compound (0.60 g, yield 65%) as colorless crystals.

後処理

  1. washwashed with water and saturated brine
  2. dry with materialdried over anhydrous magnesium sulfate
  3. concentrationconcentrated under reduced pressure
  4. washThe residue was washed with ethyl acetate

出典と根拠

ORDレコード
ord-70988a3b6cb647c2971100800c3cb15f
出典データセット
uspto-grants-2013_07
特許番号
US08492378B2

関連ノート

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