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2,6-Lutidine → HCID 178527045、化合物

HRID 1993119
ノート
印刷プレビュー

反応式

HRID 1993119 の反応式
[O-]S(C(F)(F)F)(=O)=O.[CH2:9]([O:11][P:12](C(C)(C)CN)(=[O:16])[O:13][CH2:14][CH3:15])[CH3:10].N1[C:27]([CH3:28])=[CH:26][CH:25]=[CH:24]C=1C.C(=O)([O-])[O-].[Cs+].[Cs+]>C(Cl)Cl.C(OCC)(=O)C>[PH:12](=[O:16])([O:11][CH2:9][C:10]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1)[O:13][CH2:14][C:15]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 79372,6-LutidineHCID 10796Cesium carbonateHCID 2758875TrifluoromethanesulfonateHCID 58928684Dietyl(2-amino-1,1-dimethyl-ethyl)phosphonate

生成物 1

HCID 178527045HCID 178527045、化合物

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒2 回
HCID 8857
Ethyl Acetate
溶媒

実験手順

To a solution of triflate 9 (94 mg, 0.214 mmol) in CH2Cl2 (2 mL) was added a solution of aniline 6 (100 mg, 0.173 mmol) in CH2Cl2 (2 mL) at −40° C., followed by 2,6-lutidine (0.026 mL). The mixture was warmed up to room temperature and stirred for 1 h. Cesium carbonate (60 mg) was added and the reaction mixture was stirred for additional 1 h. The mixture was diluted with ethyl acetate, washed with HCl (0.2N), dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by HPLC to afford dibenzyl phosphonate (40 mg). To a solution of this dibenzyl phosphonate in ethanol (3 mL) and ethyl acetate (1 mL) was added 10% Pd/C (40 mg). The mixture was stirred under hydrogen atmosphere (balloon) for 4 h. The reaction mixture was diluted with methanol, filtered and concentrated under reduced pressure. The residue was washed with ethyl acetate and dried to give desired product diacid 10 (20 mg). 1H NMR (CD3OD) δ 7.8 (d, 2H), 7.3 (d, 2H), 7.1 (2d, 4H), 5.6 (d, 1H), 4.9 (m, 2H), 3.4-4.0 (m, 6H), 3.9 (s, 3H), 2.53.2 (m, 9H), 2.0 (m, 2), 1.4-1.7 (m, 2H), 0.9 (2d, 6H); 31P NMR (CD3OD) δ 22.1; MS (ESI): 686 (M+H).

後処理

  1. stirringthe reaction mixture was stirred for additional 1 h
  2. washwashed with HCl (0.2N)
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by HPLC

出典と根拠

ORDレコード
ord-5322b08220cd48c082bbe4f2067177f5
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07649015B2

反応ノート

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