Diethyl Ether → HCID 178463683、化合物

HRID 853132ノート

反応式

HRID 853132 の反応式
[CH2:1]([NH:8][C@H:9]1[CH2:14][CH2:13][C@H:12]([C:15]([O:24][Si](CC)(CC)CC)([C:20]([F:23])([F:22])[F:21])[C:16]([F:19])([F:18])[F:17])[CH2:11][CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:32](OC(=O)C)(=O)[CH3:33].[NH4+].[Cl-].CCOCC>N1C=CC=CC=1>[CH2:1]([N:8]([CH2:32][CH3:33])[C@H:9]1[CH2:10][CH2:11][C@H:12]([C:15]([OH:24])([C:16]([F:18])([F:19])[F:17])[C:20]([F:21])([F:23])[F:22])[CH2:13][CH2:14]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

6

実験手順

A solution of 200 mg (0.43 mmol) of trans benzyl-[4-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-cyclohexyl]-amine (example 3.1) in 2 mL of pyridine was treated with 0.05 mL of acetic acid anhydride (0.51 mmol), stirred overnight at RT and distributed between a saturated aqueous solution of NH4Cl and Et2O. After drying of the combined organic phases over Na2SO4 and evaporation of the solvent, the residue was dissolved in 3.5 mL of THF and treated with 0.86 mL of a 1M BH3-solution in THF. The mixture was stirred at RT for 2 hrs, and the solvent evaporated. The residue was redissolved in THF treated with an excess of TBAF and solution was stirred for 2 hrs. Evaporation of the solvent and chromatography on silica gel with hexane/EtOAc 4:1 gave 64 mg (39%) of trans 2-[4-(benzyl-ethyl-amino)-cyclohexyl]-1,1,1,3,3,3-hexafluoro-propan-2-ol as a light yellow oil, MS: 384 (M+H)+.

後処理

  1. dry with materialAfter drying of the combined organic phases over Na2SO4 and evaporation of the solvent
  2. dissolutionthe residue was dissolved in 3.5 mL of THF
  3. additiontreated with 0.86 mL of a 1M BH3-solution in THF
  4. stirringThe mixture was stirred at RT for 2 hrs
  5. customthe solvent evaporated
  6. dissolutionThe residue was redissolved in THF
  7. additiontreated with an excess of TBAF and solution
  8. stirringwas stirred for 2 hrs
  9. customEvaporation of the solvent and chromatography on silica gel with hexane/EtOAc 4:1

出典と根拠

ORDレコード
ord-6468c980da9749888ec45b51cd3ee5c5
出典データセット
uspto-grants-2007_08
特許番号
US07253282B2

反応ノート

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