Tetrahydrofuran → HCID 58368641, compound

HRID 1192622Notes

Reaction equation

HRID 1192622 reaction equation
[N:1]1([CH:7]2[CH2:12][CH2:11][N:10]([C:13]3[C:14]([C:24](=O)[CH3:25])=[CH:15][C:16]([Cl:23])=[C:17]4[C:22]=3[N:21]=[CH:20][CH:19]=[CH:18]4)[CH2:9][CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C([O-])(=O)C.[NH4+].C([BH3-])#[N:33].[Na+].O1CCCC1>CO.C(#N)C>[N:1]1([CH:7]2[CH2:12][CH2:11][N:10]([C:13]3[C:14]([CH:24]([NH2:33])[CH3:25])=[CH:15][C:16]([Cl:23])=[C:17]4[C:22]=3[N:21]=[CH:20][CH:19]=[CH:18]4)[CH2:9][CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

7

Reactant 4

HCID 8028TetrahydrofuranHCID 517165Ammonium AcetateHCID 5003444Sodium cyanoborohydrideHCID 58368636HCID 58368636, compound

Product 1

HCID 58368641HCID 58368641, compound

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 6342AcetonitrileSolvent

Conditions

Temperature
65 °C

Procedure

A mixture of 1-[8-(1,4′-bipiperidin-1′-yl)-5-chloroquinolin-7-yl]ethanone (0.0165 g, 0.0444 mmol) and ammonium acetate (0.0342 g, 0.444 mmol) in methanol (0.3 mL) and acetonitrile (0.3 mL) was heated at 65° C. in a sealed tube for 1 hour. After cooling to room temperature, to the resulting mixture was added 1.0 M sodium cyanoborohydride in tetrahydrofuran (0.11 mL, 0.11 mmol). The reaction was heated at 65° C. overnight. The mixture was cooled to room temperature, quenched with sat. NaHCO3 solution and extracted with dichloromethane. The combined organic phases were dried over MgSO4 and concentrated to give the desired product. LCMS calculated for C21H30ClN4 (M+H)+: m/z=373.2; Found: 373.2.

Workup

  1. temperatureAfter cooling to room temperature, to the resulting mixture
  2. temperatureThe reaction was heated at 65° C. overnight
  3. temperatureThe mixture was cooled to room temperature
  4. customquenched with sat. NaHCO3 solution
  5. extractionextracted with dichloromethane
  6. dry with materialThe combined organic phases were dried over MgSO4
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-37e2ea1042504a4d807398b0cc8d283c
Source dataset
uspto-grants-2014_03
Patent number
US08680108B2

Reaction notes

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