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Water → 4-(4-Fluorophenyl)-7-(morpholin-4-ylmethyl)quinoline-2-carboxamide

HRID 922770
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HRID 922770 반응식
Br[CH2:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7]([C:15]3[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=3)=[CH:8][C:9]([C:13]#[N:14])=[N:10]2)=[CH:5][CH:4]=1.[NH:22]1[CH2:27][CH2:26][O:25][CH2:24][CH2:23]1.[OH-:28].[Na+].O>C(#N)C>[F:21][C:18]1[CH:19]=[CH:20][C:15]([C:7]2[C:6]3[C:11](=[CH:12][C:3]([CH2:2][N:22]4[CH2:27][CH2:26][O:25][CH2:24][CH2:23]4)=[CH:4][CH:5]=3)[N:10]=[C:9]([C:13]([NH2:14])=[O:28])[CH:8]=2)=[CH:16][CH:17]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 8083MorpholineHCID 14798Sodium HydroxideHCID 194270117-(Bromomethyl)-4-(4-fluorophenyl)quinoline-2-carbonitrile

생성물 1

HCID 895451894-(4-Fluorophenyl)-7-(morpholin-4-ylmethyl)quinoline-2-carboxamide수율 89%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

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온도
50 °C

실험 절차

To a room temperature solution of 7-(bromomethyl)-4-(4-fluorophenyl)quinoline-2-carbonitrile (2-1, 311.0 mg, 0.895 mmol, 1.0 equiv.) in acetonitrile (10.0 mL) was added morphline (85.77 mg, 0.985 mmol, 1.1 equiv.) and 5.0 M aqueous NaOH (2.69 mL, 13.43 mmol, 15 equiv.), and the resulting mixture was stirred at 50° C. for 4 days. After cooling to room temperature, water (100.0 mL) was added and the mixture was stirred for 30 minutes. A yellow solid was collected via suction filtration, washed with water, dried in vacuo. The solid was purified by reverse phase HPLC (H2O/CH3CN gradient w/0.1% TFA modifier) to afford 4-(4-fluorophenyl)-7-(morpholin-4-ylmethyl)quinoline-2-carboxamide (4-1, 291.0 mg, 80.0%) as a colorless solid. 1H NMR (500 MHz, CDCl3): δ 8.216 (s, 1H); 8.098 (br s, 2H); 7.911 (d, J=8.54 Hz, 1H); 7.642 (d, J=8.55 Hz, 1H); 7.503-7.529 (m, 2H); 7.219-7.263 (m, 2H); 5.798 (br s, 1H); 3.734 (br s, 6H); 2.528 (br s, 2H). LRMS m/z (M+H)+ 366.2 found, 366.2 required.

후처리

  1. temperatureAfter cooling to room temperature
  2. stirringthe mixture was stirred for 30 minutes
  3. filtrationA yellow solid was collected via suction filtration
  4. washwashed with water
  5. customdried in vacuo
  6. customThe solid was purified by reverse phase HPLC (H2O/CH3CN gradient w/0.1% TFA modifier)

출처 및 근거

ORD 기록
ord-f1b8ad40176646839dfd377f439b5813
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278960B2

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