Trifluoroacetic acid → HCID 58497698, compound

HRID 1616677Notes

Reaction equation

HRID 1616677 reaction equation
[CH:1]1([C:6](Cl)=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.FC(F)(F)C(O)=O.[CH3:16][O:17][C:18]1[C:32]([N+:33]([O-:35])=[O:34])=[CH:31][C:21]2[CH2:22][C@@H:23]3[C@H:28]([CH3:29])[C@:27]([CH3:30])([C:20]=2[C:19]=1[N+:36]([O-:38])=[O:37])[CH2:26][CH2:25][NH:24]3.C([O-])([O-])=O.[Na+].[Na+]>ClCCl.C(N(CC)CC)C>[CH:1]1([C:6]([N:24]2[CH2:25][CH2:26][C@:27]3([CH3:30])[C@@H:28]([CH3:29])[C@H:23]2[CH2:22][C:21]2[CH:31]=[C:32]([N+:33]([O-:35])=[O:34])[C:18]([O:17][CH3:16])=[C:19]([N+:36]([O-:38])=[O:37])[C:20]=23)=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

7

Procedure

Cyclopentanecarbonyl chloride (0.12 g) is added to the trifluoroacetic acid salt of (2R,6R,11R)-8-methoxy-6,11-dimethyl-7,9-dinitro-1,2,3,4,5,6-hexahydro-2,6-methano-benzo[d]azocine (0.43 g) and triethylamine (0.31 mL) dissolved in dichloromethane (10 mL). The resulting solution is stirred at room temperature overnight. Then, aqueous Na2CO3 solution is added and the resulting mixture is extracted with dichloromethane. The combined extracts are washed with water and dried (Na2SO4) and the solvent is evaporated. The residue is purified by HPLC on reversed phase (MeCN/H2O) to give the product as a white solid.

Workup

  1. extractionthe resulting mixture is extracted with dichloromethane
  2. washThe combined extracts are washed with water
  3. dry with materialdried (Na2SO4)
  4. customthe solvent is evaporated
  5. customThe residue is purified by HPLC on reversed phase (MeCN/H2O)

Sources & evidence

ORD record
ord-c568b731ba454d45bf13ae204a013a5c
Source dataset
uspto-grants-2014_07
Patent number
US08765780B2

Reaction notes

Loading…