Tributylphosphine → 3-{4-[6-(4-Trifluoromethyl-phenyl)-pyridin-3-ylmethoxy]-benzoylamino}-propionic acid methyl ester
反応式
[F:1][C:2]([F:18])([F:17])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:14]=[CH:13][C:12]([CH2:15][OH:16])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.N(C(N1CCCCC1)=O)=NC(N1CCCCC1)=O.C(P(CCCC)CCCC)CCC.[CH3:50][O:51][C:52](=[O:65])[CH2:53][CH2:54][NH:55][C:56](=[O:64])[C:57]1[CH:62]=[CH:61][C:60](O)=[CH:59][CH:58]=1>C1COCC1.C1(C)C=CC=CC=1>[CH3:50][O:51][C:52](=[O:65])[CH2:53][CH2:54][NH:55][C:56](=[O:64])[C:57]1[CH:62]=[CH:61][C:60]([O:16][CH2:15][C:12]2[CH:13]=[N:14][C:9]([C:6]3[CH:5]=[CH:4][C:3]([C:2]([F:17])([F:1])[F:18])=[CH:8][CH:7]=3)=[CH:10][CH:11]=2)=[CH:59][CH:58]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of [6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-methanol (120 mg, 0.47 mmol) in THF (2 mL) and toluene (4 mL) is added 1,1′-(azodicarbonyl)dipiperidine (ADDP, 179.5 mg, 0.71 mmol) at 0° C., followed by the addition of tributylphosphine (0.18 mL, 0.71 mmol) and 3-(4-hydroxy-benzoylamino)-propionic acid methyl ester (127 mg, 0.57 mmol). The reaction mixture is warmed up to room temperature and stirred overnight. The mixture is loaded on silica gel, eluted with hexanes with a gradient from 0% of ethyl acetate to 50% of ethyl acetate giving 3-{4-[6-(4-trifluoromethyl-phenyl)-pyridin-3-ylmethoxy]-benzoylamino}-propionic acid methyl ester. The ester product is taken into ethanol (2 mL), treated with sodium hydroxide (5N aqueous, 1 mL) for 3 h at room temperature. The mixture is concentrated, diluted with ethyl acetate, acidified with 5 N HCl (1.1 mL), extracted with ethyl acetate. The organic layers are dried and concentrated giving 3-{4-[6-(4-Trifluoromethyl-phenyl)-pyridin-3-ylmethoxy]-benzoylamino}-propionic acid (33 mg). MS (ES): 443.2 [M+H]−.
後処理
- washeluted with hexanes with a gradient from 0% of ethyl acetate to 50% of ethyl acetate
出典と根拠
- ORDレコード
- ord-c1a383c177264f37b831c84bfe3c83cd
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US07989457B2
反応ノート
読み込み中…