Cesium carbonate → HCID 178490342, compound

HRID 130887

Reaction equation

HRID 130887 reaction equation
[NH2:1][C@H:2]1[CH2:7][CH2:6][C@H:5]([OH:8])[CH2:4][CH2:3]1.C([O-])([O-])=O.[Cs+].[Cs+].Cl[CH2:16][CH2:17][C:18]1[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=1>CN(C=O)C>[CH3:25][O:24][C:21]1[CH:22]=[CH:23][C:18]([CH2:17][CH2:16][NH:1][C@H:2]2[CH2:7][CH2:6][C@H:5]([OH:8])[CH2:4][CH2:3]2)=[CH:19][CH:20]=1

Participants

5

Procedure

Heat a mixture of (±)-(trans)-4-aminocyclohexanol (607 m, 5.3 mmol), Cs2CO3 (4.300 g, 13.2 mmol), and 1-(2-chloroethyl)-4-methoxybenzene (0.8 mL) in DMF (10 mL) at 100° C. for 19 hours. Quench the reaction with saturated aqueous NH4Cl (40 mL). Adjust the pH to alkaline and concentrate to dryness. Suspend the residue in 50:40:10 EtOAc/CH2Cl2/2.0 M NH3 in MeOH and stir vigorously for 1 hour. Decant the supernatant. Suspend the residue in 10:90 2.0 M NH3 in MeOH/CH2Cl2 for 30 minutes and filter. Combine the organic layers, concentrate, and purify by flash chromatography, eluting with 75:15:10 EtOAc/CH2Cl2/2.0 M NH3 in MeOH to afford the title compound (258.3 mg, 20%): MS ES+ 250.0 (M+H)+, HPLC [YMC-Pack Pro C-18 (150×4.6 mm, S-5 microm), acetonitrile in water containing 0.01% concentrated HCl at 1.0 mL/min, 30-99% over 19 min], tR=1.96 min, 100% purity.

Workup

  1. temperatureHeat
  2. customQuench
  3. customthe reaction with saturated aqueous NH4Cl (40 mL)
  4. concentrationconcentrate to dryness
  5. customDecant the supernatant
  6. customfor 30 minutes
  7. filtrationfilter
  8. concentrationconcentrate
  9. custompurify by flash chromatography
  10. washeluting with 75:15:10 EtOAc/CH2Cl2/2.0 M NH3 in MeOH

Sources & evidence

ORD record
ord-78c87ca05a644d368f1556e67a05a93c
Source dataset
uspto-grants-2008_06
Patent number
US07381719B2

Linked notes

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