Acetic Acid → HCID 12015899、化合物
反応式
[C:1]([O:5][C:6](=[O:27])[CH2:7][O:8][C:9]1[CH:17]=[CH:16][CH:15]=[C:14]2[C:10]=1[CH:11]=[C:12]([CH2:25][CH3:26])[N:13]2[CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)([CH3:4])([CH3:3])[CH3:2].ClC(Cl)(Cl)COC(N=[N:35][C:36]([O:38]CC(Cl)(Cl)Cl)=O)=O.C(O)(=O)C.C[Si]([N:54]=C=O)(C)C>C(OCC)C.C1COCC1.O.[Zn]>[C:1]([O:5][C:6](=[O:27])[CH2:7][O:8][C:9]1[CH:17]=[CH:16][CH:15]=[C:14]2[C:10]=1[C:11]([NH:35][C:36]([NH2:54])=[O:38])=[C:12]([CH2:25][CH3:26])[N:13]2[CH2:18][C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)([CH3:4])([CH3:3])[CH3:2]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 4
実験手順
A solution of 2.3 g (6.3 mmol) [[2-ethyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]acetic acid tert-butyl ester and 4.8 g (12.6 mmol) bis(2,2,2-trichloroethyl)-azodicarboxylate in diethyl ether is stirred for 24 hours at room temperature. The resulting solid is filtered and vacuum dried. This adduct (1 g, 1.3 mmol) is dissolved in 10 mL of THF and treated with zinc (1 g) and glacial acetic acid (0.5 mL) . After stirring for 30 minutes at room temperature an excess of trimethyisiiyiisocyanate in 1 mL, of THF is added and stirring is continued at room temperature for 18 hours. The mixture is diluted with water and extracted with ethyl acetate. The organic layer is washed with brine, dried over MgSO4 and concentrated to dryness to give 0.385 g (69% yield) of the subtitled material. Mass spectrum: 423.
後処理
- filtrationThe resulting solid is filtered
- customvacuum dried
- extractionextracted with ethyl acetate
- washThe organic layer is washed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated to dryness
出典と根拠
- ORDレコード
- ord-b91f25028a20462089708c4cb9447e51
- 出典データセット
- uspto-grants-2002_08
- 特許番号
- US06436983B1
反応ノート
読み込み中…