反応式
[F:1][C:2]([F:19])([F:18])[C:3]1[CH:11]=[C:10]([C:12]([F:15])([F:14])[F:13])[CH:9]=[C:8]([O:16][CH3:17])[C:4]=1[C:5](O)=[O:6].C(N(CC)C(C)C)(C)C.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.[C:53]1([CH:59]([NH2:69])[C:60]2([N:64]3[CH2:68][CH2:67][CH2:66][CH2:65]3)[CH2:63][O:62][CH2:61]2)[CH:58]=[CH:57][CH:56]=[CH:55][CH:54]=1>CN(C)C=O>[CH3:17][O:16][C:8]1[CH:9]=[C:10]([C:12]([F:13])([F:14])[F:15])[CH:11]=[C:3]([C:2]([F:1])([F:18])[F:19])[C:4]=1[C:5]([NH:69][CH:59]([C:53]1[CH:58]=[CH:57][CH:56]=[CH:55][CH:54]=1)[C:60]1([N:64]2[CH2:65][CH2:66][CH2:67][CH2:68]2)[CH2:63][O:62][CH2:61]1)=[O:6]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
2,4-Bis(trifluoromethyl)-6-methoxybenzoic acid (155 mg, 0.538 mmol) was dissolved in 2 mL dimethylformamide. N,N-Diisopropyl ethyl amine (78 mg, 0.605 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (205 mg, 0.539 mmol) were added. After 5 minutes of stirring at room temperature C-phenyl-C-(3-pyrrolidin-1-yl-oxetan-3-yl)-methylamine (intermediate B) (125 mg, 0.539 mmol) in 2 mL dimethylformamide was added. The reaction mixture was stirred at room temperature overnight. The solvent was evaporated off. The residue was taken up in 2N sodium carbonate solution and ethyl acetate and was extracted three times with ethyl acetate. The combined organic phases were dried on sodium sulfate, filtered and evaporated. Purification of the residue by flash chromatography on silica gel (heptane/ethyl acetate 1:0-1:1) yielded 2-methoxy-N-[phenyl-(3-pyrrolidin-1-yl-oxetan-3-yl)-methyl]-4,6-bis-trifluoromethyl-benzamide as an off-white solid (173 mg, 64%), MS: m/e=503.2 [(M+H)+].
後処理
- additionwas added
- customThe solvent was evaporated off
- extractionethyl acetate and was extracted three times with ethyl acetate
- customThe combined organic phases were dried on sodium sulfate
- filtrationfiltered
- customevaporated
- customPurification of the residue by flash chromatography on silica gel (heptane/ethyl acetate 1:0-1:1)
出典と根拠
- ORDレコード
- ord-794e7b21d4d44e98a0a40b7aaad0f9ed
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08063098B2
関連ノート
読み込み中…