Reaktion #42142

ord-c96354509dec4955bc0831af79a7db73

Reaktionsgleichung

COC(=O)c1ccc(C(=O)O)c(OC)c1
2-methoxyterephthalic acid 4-methyl ester
ClCCCl
EDC
On1nnc2cccnc21
HOAt
CCN(C(C)C)C(C)C
DIPEA
CNCCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1
biphenyl-2-ylcarbamic acid 1-(2-methylaminoethyl)piperidin-4-yl ester
COC(=O)c1ccc(C(=O)N(C)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)c(OC)c1
title intermediate
Ausbeute 89.0%
COC(=O)c1ccc(C(=O)N(C)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)c(OC)c1
N-{2-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]ethyl}-3-methoxy-N-methylterephthalamic Acid Methyl Ester
Ausbeute 89.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with water (100 mL), 1N HCl (100 mL), 1N NaOH (100 mL), brine (100 mL)
  2. 2
    Trocknendried over MgSO4
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated

Vorschrift

To a stirred solution of 2-methoxyterephthalic acid 4-methyl ester (450 mg, 2.1 mmol; prepared as described in Preparation 18) in DMF (10 mL) was added EDC (630 mg, 3.3 mmol), HOAt (2.4 mL, 1.18 mmol, 0.5M in DMF) and DIPEA (1.3 mL, 7.05 mmol). When the mixture was homogenous, a solution of biphenyl-2-ylcarbamic acid 1-(2-methylaminoethyl)piperidin-4-yl ester (830 mg, 2.4 mmol; prepared as described in Preparation 4) was added slowly. The reaction mixture was stirred at room temperature for 16 hours and then washed with water (100 mL), 1N HCl (100 mL), 1N NaOH (100 mL), brine (100 mL), dried over MgSO4, filtered and concentrated to afford the title intermediate in 89% yield (1.04 g, 1.9 mmol). MS m/z: [M+H+] calcd for C31H35N3O6, 545.6; found, 546.6.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728144B2uspto-grants-2010_06