Trifluoroacetic acid → HCID 57418643、化合物

HRID 2114384ノート

反応式

HRID 2114384 の反応式
[C:1]1([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:6]=[CH:5][C:4]([CH:7]([NH:14][CH3:15])[CH2:8][N:9]2[CH2:13][CH2:12][CH2:11][CH2:10]2)=[CH:3][CH:2]=1.[CH2:22]([O:24][C:25]([C:27]1[CH:28]=[CH:29][C:30]2[O:35][CH2:34][C:33](=[O:36])[N:32]([CH2:37][C:38]([OH:40])=O)[C:31]=2[CH:41]=1)=[O:26])[CH3:23].C(N(CC)CC)C.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.FC(F)(F)C(O)=O>C(Cl)Cl.CC#N.O>[C:1]1([C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:6]=[CH:5][C:4]([CH:7]([N:14]([CH3:15])[C:38](=[O:40])[CH2:37][N:32]2[C:31]3[CH:41]=[C:27]([C:25]([O:24][CH2:22][CH3:23])=[O:26])[CH:28]=[CH:29][C:30]=3[O:35][CH2:34][C:33]2=[O:36])[CH2:8][N:9]2[CH2:13][CH2:12][CH2:11][CH2:10]2)=[CH:3][CH:2]=1

参加物

8

反応物 5

HCID 6422Trifluoroacetic acidHCID 8471TriethylamineHCID 151348Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 27567161-([1,1'-Biphenyl]-4-yl)-N-methyl-2-(pyrrolidin-1-yl)ethan-1-amineHCID 57457165HCID 57457165、化合物

生成物 1

HCID 57418643HCID 57418643、化合物収率 77.8%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒2 回HCID 18373917Acetonitrile--water (1/1)溶媒

実験手順

[1-(4-biphenylyl)-2-(1-pyrrolidinyl)ethyl]methylamine (0.5 g, 1.8 mmol) and {6-[(ethyloxy)carbonyl]-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl}acetic acid (0.63 g, 2.0 mmol) were dissolved in 10 mL of methylene chloride. Triethylamine (1.0 mL, 7.1 mmol) was delivered to the room temperature mixture, and the solution was allowed to stir for several minutes before a separate solution of 1H-1,2,3-benzotriazol-1-yloxy-tris(dimethylamino)-phosphonium hexafluorophosphate (BOP reagent, 0.89 g, 2.0 mmol) dissolved in 4 mL of methylene chloride was added at room temperature to the mixture. The reaction was maintained at that temperature for 72 hours, before it was determined to be complete by LCMS (two Aquasil C18, 20×1 mm columns were run in sequence, 4 minutes at 0.1 mL/min, 1-99% CH3CN/H2O with 0.018% trifluoroacetic acid, ES) Rt=2.7 min and m/e 542 [M+1]+. Solvent was removed by rotary evaporation and the crude residue was purified by prep HPLC (Waters, 50×100 mm, 84 mL/min, A: acetonitrile B: water (pH=10, NH4OH), A: 10 to 99% over 15 min, UV detection at 214 nm) to give the title compound (0.75 g. 1.4 mmol, 77%) as a pale yellow amorphous solid. MS (ES) m/e 542 [M+H]+.

後処理

  1. customwas delivered to the room temperature mixture
  2. additionwas added at room temperature to the mixture
  3. temperatureThe reaction was maintained at that temperature for 72 hours, before it
  4. customSolvent was removed by rotary evaporation
  5. customthe crude residue was purified by prep HPLC (Waters, 50×100 mm, 84 mL/min

出典と根拠

ORDレコード
ord-e5535e73a2104af7a5e01095fa71e72c
出典データセット
uspto-grants-2008_10
特許番号
US07432258B2

反応ノート

読み込み中…