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Imidazole → 2-Chloro-3-(iodomethyl)-8-methylquinoline

HRID 1948730
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HRID 1948730 반응식
[Cl:1][C:2]1[C:11]([CH2:12]O)=[CH:10][C:9]2[C:4](=[C:5]([CH3:14])[CH:6]=[CH:7][CH:8]=2)[N:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[I:34]I.N1C=CN=C1>C(Cl)Cl>[Cl:1][C:2]1[C:11]([CH2:12][I:34])=[CH:10][C:9]2[C:4](=[C:5]([CH3:14])[CH:6]=[CH:7][CH:8]=2)[N:3]=1
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참가 물질

6

반응물 4

HCID 795ImidazoleHCID 807IodineHCID 11776TriphenylphosphineHCID 865104(2-Chloro-8-methylquinolin-3-yl)methanol

생성물 1

HCID 873073252-Chloro-3-(iodomethyl)-8-methylquinoline수율 72%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of (2-chloro-8-methylquinolin-3-yl)methanol (2.0 g, 10 mmol) in DCM (200 mL) were added triphenylphosphine (2.6 g, 10 mmol), iodine (2.6 g, 10 mmol) and imidazole (0.7 g, 10 mmol) and the reaction mixture was stirred for 2 h at r.t. The mixture was washed with water (50 mL) and the organic layer was separated, dried and concentrated in vacuo. Purification by column chromatography (SiO2, 50% Et2O in heptane) gave the title compound as a brown solid (2.2 g, 72%). δH (CDCl3) 8.17 (s, 1H), 7.62 (d, J 9 Hz, 1H), 7.55 (d, J 9 Hz, 1H), 7.45 (t, J 9 Hz, 1H), 4.68 (s, 2H), 2.75 (s, 3H). LCMS (ES+) 318.0, 320.0 (M+H)+, RT 4.53 minutes (Method 3).

후처리

  1. washThe mixture was washed with water (50 mL)
  2. customthe organic layer was separated
  3. customdried
  4. concentrationconcentrated in vacuo
  5. customPurification by column chromatography (SiO2, 50% Et2O in heptane)

출처 및 근거

ORD 기록
ord-96f0eca424fe491285d6ced19efc7790
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399483B2

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