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Ammonia → 3-(3-Bromo-4-fluorophenyl)propanimidamide hydrochloride

HRID 474555
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HRID 474555 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH2:9][CH2:10][C:11]#[N:12])[CH:5]=[CH:6][C:7]=1[F:8].CO.C([Cl:18])(=O)C.[NH3:19]>C1(C)C=CC=CC=1>[ClH:18].[Br:1][C:2]1[CH:3]=[C:4]([CH2:9][CH2:10][C:11](=[NH:19])[NH2:12])[CH:5]=[CH:6][C:7]=1[F:8]
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참가 물질

6

반응물 4

HCID 222AmmoniaHCID 887MethanolHCID 6367Acetyl chlorideHCID 534343013-(3-Bromo-4-fluorophenyl)propanenitrile

생성물 1

HCID 677757593-(3-Bromo-4-fluorophenyl)propanimidamide hydrochloride수율 93%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of 3-(3-bromo-4-fluorophenyl)propanenitrile (5.0 g, 21.05 mmol) in toluene (20 mL) and methanol (6.32 mL, 156 mmol) at 0° C. was added acetyl chloride (7.51 mL, 105 mmol) dropwise over 5 min. The reaction mixture was allowed to warm to room temperature and stirred for 2 h. The mixture was cooled to 0° C. by an ice bath, to which ammonia (30.1 mL, 210 mmol) was added dropwise. The reaction mixture was stirred at room temperature overnight. The mixture was filtered, and the filtrate was concentrated to give a crude product. Recrystallization from toluene/methanol (1:1) then afforded the title compound as a white solid (5.2 g, 93% yield). LCMS: rt=1.18 min, [M+H+]=245

후처리

  1. additionwas added dropwise
  2. stirringThe reaction mixture was stirred at room temperature overnight
  3. filtrationThe mixture was filtered
  4. concentrationthe filtrate was concentrated
  5. customto give a crude product
  6. customRecrystallization from toluene/methanol (1:1)

출처 및 근거

ORD 기록
ord-c466bac0dd324917b99b21f04c248937
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637536B2

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