반응 #2446111

ord-ae1e1b1119c54cfaa846259f4c90670c

반응 방정식

C[Si](C)(C)[N-][Si](C)(C)C.[K+]
Potassium bis(trimethylsilyl)amide
O=C([O-])O.[Na+]
Sodium bicarbonate
ClCCl.O=C(O)C(F)(F)F
DCM trifluoroacetic acid
NC(=O)Cl
carbamoyl chloride
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314
Oxycodone
COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)[C@@H](C2)N(C)CC[C@]314
oxycodone
CN(CCN)C(=O)[O-]
N-methyl-N-(2-amino)ethylcarbamate
O=C(O)C(F)(F)F
TFA

용매

반응 조건

온도
-10°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타in dry
  2. 2
    기타degassed tetrahydrofuran (120 mL)
  3. 3
    workup.STIRRINGThe mixture was stirred at −5° C. for 30 min
  4. 4
    workup.STIRRINGThe reaction was stirred at room temperature for 2 h
  5. 5
    농축The mixture was concentrated under vacuum to half of its initial volume
  6. 6
    workup.ADDITIONEtOAc (50 mL) was added
  7. 7
    기타layers were separated
  8. 8
    세척The organic phase was further washed with water (3×20 mL) and brine (40 mL)
  9. 9
    농축was concentrated
  10. 10
    기타The residue was purified by silica gel chromatography
  11. 11
    기타to afford a white foam in 55% yield (7.0 g, 13.4 mmol)
  12. 12
    workup.STIRRINGstirred for 1 h
  13. 13
    농축The solution was then concentrated under vacuum

실험 절차

Oxycodone free base (6.5 g, 20.6 mmol) was dissolved in dry, degassed tetrahydrofuran (120 mL), and the mixture was cooled to −10° C. using a dry ice/acetone bath. Potassium bis(trimethylsilyl)amide (KHMDS) (103.0 mL, 51.6 mmol, 0.5 M in toluene) was added via cannula. The mixture was stirred under N2 at below −5° C. for 30 min. N,N-Bis(tert-butyl) N′-2-(chlorocarbonyl(methyl)amino)ethylcarbamate (8.0 g, 23.7 mmol), (Compound C) in THF (30 mL) was then added via cannula over 15 min. The mixture was stirred at −5° C. for 30 min. Another portion of carbamoyl chloride (4.0 g, 11.9 mmol) in THF (10 mL) was added. The reaction was stirred at room temperature for 2 h. Sodium bicarbonate (10 mL, sat. aq.) was added. The mixture was concentrated under vacuum to half of its initial volume. EtOAc (50 mL) was added, and layers were separated. The organic phase was further washed with water (3×20 mL) and brine (40 mL), and then was concentrated. The residue was purified by silica gel chromatography, using DCM/MeOH (gradient 100/1 to 100/15) to afford a white foam in 55% yield (7.0 g, 13.4 mmol). This material was dissolved in a 1:1 mixture of DCM/trifluoroacetic acid (TFA) (20 mL/20 mL) at room temperature and stirred for 1 h. The solution was then concentrated under vacuum to afford a TFA salt of oxycodone 6-(N-methyl-N-(2-amino)ethylcarbamate (Compound KC-19) as a thick oil (7.3 g, 11.4 mmol, 99% purity). MS: (m/z) calc: 415.2, observed (M+H+) 416.5.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08685916B2uspto-grants-2014_04