Hydrochloric Acid → HCID 86622859, compound

HRID 1013124Notes

Reaction equation

HRID 1013124 reaction equation
ClC1C=CC2CCN(C(=O)C(F)(F)F)CCC=2C=1OS(C(F)(F)F)(=O)=O.CC1(CCCN)OCCO1.C1(P(C2C=CC=CC=2)C2C=CC3C(=CC=CC=3)C=2C2C3C(=CC=CC=3)C=CC=2P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(=O)([O-])[O-].[Cs+].[Cs+].[Cl:89][C:90]1[CH:106]=[CH:105][C:93]2[CH2:94][CH2:95][N:96]([C:99](=[O:104])[C:100]([F:103])([F:102])[F:101])[CH2:97][CH2:98][C:92]=2[C:91]=1[NH:107][CH2:108][CH2:109][CH2:110][C:111]1([CH3:116])OCCO1.Cl.C([BH3-])#N.[Na+]>C1(C)C=CC=CC=1.CCOC(C)=O.C(Cl)Cl.C(OCC)C.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].CO>[Cl:89][C:90]1[CH:106]=[CH:105][C:93]2[CH2:94][CH2:95][N:96]([C:99](=[O:104])[C:100]([F:101])([F:103])[F:102])[CH2:97][CH2:98][C:92]=2[C:91]=1[N:107]1[CH2:108][CH2:109][CH2:110][CH:111]1[CH3:116]

Participants

14

Conditions

Temperature
95 °C

Procedure

Place 7-chloro-3-(2,2,2-trifluoroacetyl)-6-trifluoromethanesulfonyloxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine (prepared essentially as described in Preparation 1) (3 g, 7.08 mmol) in toluene (60 mL) with 3-(2-methyl-[1,3]dioxolan-2-yl)-propylamine (prepared essentially as described in Preparation 38) (3.08 g, 21.24 mmol), tris(dibenzylideneacetone)dipalladium (1.3 g, 1.42 mmol), racemic 2,2′-bis(diphenylphosphino)-1,1′-binapthyl (1.77 g, 2.84 mmol), and cesium carbonate (3.3 g, 9.91 mmol) and heat for 16 h at 95° C. in a sealed tube. Cool the reaction to RT, dilute with EtOAc (600 mL) and filter. Concentrate the filtrate and purify (silica gel chromatography, eluting with 10:90 to 25:75 EtOAc:hexanes) to give the crude product as an orange oil (1.72 g). Dissolve 7-chloro-3-(2,2,2-trifluoroacetyl)-6-[3-(2-methyl[1,3]dioxolan-2-yl)-propylamino]-2,3,4,5-tetrahydro-1H-benzo[d]azepine (1.72 g, 4.09 mmol) in DCM (20 mL) and add methanol (2 mL) and 2 N HCl in diethyl ether (20 mL) and stir at RT for 3 h. Concentrate and dissolve the residue in acetic acid (30 mL) and add sodium cyanoborohydride (1.28 g, 20.43 mmol). Stir the reaction at RT for 0.5 h then concentrate to remove the acetic acid. Dissolve the residue in DCM (200 mL) and extract with saturated aqueous sodium bicarbonate solution (400 mL), Extract the aqueous layer with DCM (100 mL) and combine the organic fractions, dry (sodium sulfate), concentrate and purify (silica gel chromatography, eluting with 10:90 EtOAc:hexanes) to give the title compound as a foam (1.2 g, 81%).

Workup

  1. customprepared essentially
  2. temperatureCool
  3. customthe reaction to RT
  4. filtrationfilter
  5. concentrationConcentrate the filtrate
  6. custompurify
  7. wash(silica gel chromatography, eluting with 10:90 to 25:75 EtOAc:hexanes)
  8. customto give the crude product as an orange oil (1.72 g)
  9. concentrationConcentrate
  10. dissolutiondissolve the residue in acetic acid (30 mL)
  11. stirringStir
  12. customthe reaction at RT for 0.5 h
  13. concentrationthen concentrate
  14. customto remove the acetic acid
  15. dissolutionDissolve the residue in DCM (200 mL)
  16. extractionextract with saturated aqueous sodium bicarbonate solution (400 mL)
  17. extractionExtract the aqueous layer with DCM (100 mL)
  18. dry with materialdry (sodium sulfate)
  19. concentrationconcentrate
  20. custompurify
  21. wash(silica gel chromatography, eluting with 10:90 EtOAc:hexanes)

Sources & evidence

ORD record
ord-c22474ca54ec40f59dfcd8a782ea4786
Source dataset
uspto-grants-2011_07
Patent number
US07981882B2

Reaction notes

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