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

HRID 1276620
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HRID 1276620 반응식
[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]
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참가 물질

4

반응물 2

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

생성물 1

HCID 221165242-Amino-5-iodo-N-propylbenzamide수율 74.1%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-ba8aa42850ad44af9b79907d0b0c5476
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06166208

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