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Propylamine → 2-Amino-5-iodo-N-propylbenzamide

HRID 1276620
ノート
印刷プレビュー

反応式

HRID 1276620 の反応式
[CH2:1]([NH2:4])[CH2:2][CH3:3].[I:5][C:6]1[CH:7]=[CH:8][C:9]2[NH:14]C(=O)O[C:11](=[O:16])[C:10]=2[CH:17]=1>N1C=CC=CC=1>[NH2:14][C:9]1[CH:8]=[CH:7][C:6]([I:5])=[CH:17][C:10]=1[C:11]([NH:4][CH2:1][CH2:2][CH3:3])=[O:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 7852PropylamineHCID 2944806-iodo-2H-3,1-benzoxazine-2,4(1H)-dione

生成物 1

HCID 221165242-Amino-5-iodo-N-propylbenzamide収率 74.1%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

Propylamine (1.2 g, 20.3 mmol) and 6-iodo-2H-3,1-benzoxazine-2,4(1H)-dione (5.0 g, 17.3 mmol) were combined in pyridine (85 mL) and stirred at room temperature for 24 h. The reaction was concentrated under reduced pressure and the resulting residue was partitioned between ethyl acetate (200 mL) and 5% hydrochloric acid (200 mL). The phases were separated and the organic phase was washed with 1N sodium hydroxide, water, and brine. Drying over anhydrous sodium sulfate and evaporation under reduced pressure afforded 3.9 g of the title compound, 1H NMR (300 MHz, CDCl3): δ0.99 (t,3H1); 1.63 (m,2H); 3.35 (m,2H); 5.52 (br s,2H); 5.95 (br s,1H); 6.47 (d, 1H); 7.42 (dd,1H); 7.55(d,1H).

後処理

  1. concentrationThe reaction was concentrated under reduced pressure
  2. customthe resulting residue was partitioned between ethyl acetate (200 mL) and 5% hydrochloric acid (200 mL)
  3. customThe phases were separated
  4. washthe organic phase was washed with 1N sodium hydroxide, water, and brine
  5. dry with materialDrying over anhydrous sodium sulfate and evaporation under reduced pressure

出典と根拠

ORDレコード
ord-ba8aa42850ad44af9b79907d0b0c5476
出典データセット
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06166208

反応ノート

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