6-[5-(3-Chloropropyl)imidazol-1-ylmethyl]biphenyl-3-carbonitrile → HCID 69438002、化合物

HRID 1877963ノート

反応式

HRID 1877963 の反応式
Cl[CH2:2][CH2:3][CH2:4][C:5]1[N:9]([CH2:10][C:11]2[C:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:15][C:14]([C:23]#[N:24])=[CH:13][CH:12]=2)[CH:8]=[N:7][CH:6]=1.CC([O-])(C)C.[K+].C1COCC1>C1COCC1>[CH2:6]1[CH:5]2[CH2:4][CH2:3][CH2:2][CH:10]([C:11]3[C:16]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)=[CH:15][C:14]([C:23]#[N:24])=[CH:13][CH:12]=3)[N:9]2[CH:8]=[N:7]1

参加物

4

反応物 2

HCID 588270706-[5-(3-Chloropropyl)imidazol-1-ylmethyl]biphenyl-3-carbonitrileHCID 66863523KOtBu THF

生成物 1

HCID 69438002HCID 69438002、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 6-[5-(3-chloropropyl)imidazol-1-ylmethyl]biphenyl-3-carbonitrile (1.0 g, 3.0 mmol) in THF (16 mL) at 0° C. is added t-BuOK/THF (1.0 M, 6 mL, 6.0 mmol). The mixture is warmed up to ambient temperature and stirred for 2 h. The reaction mixture is quenched by saturated aqueous NH4Cl and partitioned between CH2Cl2 and brine. The organic layer is washed by brine, dried over anhydrous Na2SO4 and concentrated to give the crude oil, which is subjected to flash chromatography (silica gel) eluting with MeOH:CH2Cl2 to yield the desired compound. MS (ESI) m/z 300 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 1.50-1.66 (m, 1 H), 1.73-1.83 (m, 1 H), 1.83-1.95 (m, 1 H), 1.95-2.16 (m, 1 H), 2.68-2.95 (m, 2 H), 5.28 (dd, J=8.5, 5.2 Hz, 1 H), 6.83 (s, 1 H), 7.01-7.15 (m, 2 H), 7.27-7.35 (m, 2 H), 7.43-7.54 (m, 3 H), 7.58 (s, 1 H), 7.62 (d, J=8.3 Hz, 1 H). Resolution of the enantiomers of the title compound is achieved by Chiral HPLC using the ChiralPak AD column with a 20% IPA/Hexane mobile phase.

後処理

  1. customThe reaction mixture is quenched by saturated aqueous NH4Cl
  2. custompartitioned between CH2Cl2 and brine
  3. washThe organic layer is washed by brine
  4. dry with materialdried over anhydrous Na2SO4
  5. concentrationconcentrated
  6. customto give the crude oil, which
  7. washeluting with MeOH

出典と根拠

ORDレコード
ord-93047093a9b548cfb1d55e39d1bfe06b
出典データセット
uspto-grants-2012_11
特許番号
US08314097B2

反応ノート

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