Trifluoroacetic acid → HCID 131734160, compound
Reaction equation
[CH:1]1([CH:7]2[CH:16]3[CH2:17][CH2:18][CH2:19][O:20][CH:15]3[C:14]3[CH:13]=[C:12]([NH:21]C(=O)[O-])[CH:11]=[CH:10][C:9]=3[NH:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(O)(C(F)(F)F)=O.[OH-].[Na+]>C(Cl)Cl>[CH:1]1([CH:7]2[CH:16]3[CH2:17][CH2:18][CH2:19][O:20][CH:15]3[C:14]3[CH:13]=[C:12]([NH2:21])[CH:11]=[CH:10][C:9]=3[NH:8]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To an ice-cooled solution of tert-butyl(4aSR*,5SR*,10bSR*)-5-cyclohexyl-3,4,4a,5,6,10b-hexahydro-2H-pyrano[3,2-c]quinolin-9-ylcarbamate (prepared according to the method described in example 1) (227 mg, 0.587 mmol) in CH2Cl2 (5 mL) under argon atmosphere was added TFA (1.5 mL) dropwise. The reaction solution was allowed to reach r.t. and stirred overnight. The mixture was cooled down and 0.5 N NaOH solution was added until basic pH. The product was extracted with CH2Cl2 three times. The combined organic fractions were washed with sat. NaCl solution, dried over Na2SO4, and the solvent removed under reduced pressure after filtration giving (4aSR*,5SR*,10bSR*)-5-cyclohexyl-3,4,4a,5,6,10b-hexahydro-2H-pyrano[3,2-c]quinolin-9-amine (145 mg, 86%) as orange viscous solid. The product was used without further purification.
Workup
- customprepared
- customto reach r.t.
- temperatureThe mixture was cooled down
- extractionThe product was extracted with CH2Cl2 three times
- washThe combined organic fractions were washed with sat. NaCl solution
- dry with materialdried over Na2SO4
- customthe solvent removed under reduced pressure
- filtrationafter filtration
Sources & evidence
- ORD record
- ord-85fc99b733c3464480ce079ec9126751
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09408842B2
Reaction notes
Loading…