Reaktion #42134

ord-80aa58dd0d9b402ebe4d56603735b1eb

Reaktionsgleichung

O=Cc1ccc(C(=O)O)cc1
4-carboxybenzaldehyde
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
NCCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1
biphenyl-2-ylcarbamic acid 1-(2-aminoethyl)piperidin-4-yl ester
CCN(C(C)C)C(C)C
DIPEA
O=Cc1ccc(C(=O)NCCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1
title intermediate
Ausbeute 92.2%
O=Cc1ccc(C(=O)NCCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1
Biphenyl-2-ylcarbamic Acid 1-[2-(4-Formylbenzoylamino)ethyl]piperidin-4-yl Ester
Ausbeute 92.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe resulting mixture was stirred at room temperature for 2 hours
  2. 2
    Waschenwashed with saturated sodium bicarbonate (150 mL) and brine (150 mL)
  3. 3
    TrocknenThe organic layer was dried over MgSO4
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated

Vorschrift

A mixture of 4-carboxybenzaldehyde (0.95 g, 6.35 mmol) and HATU (3.02 g, 7.94 mmol) in 55 mL of DCM was stirred at room temperature for 1 hour and then biphenyl-2-ylcarbamic acid 1-(2-aminoethyl)piperidin-4-yl ester (3 g, 5.29 mmol; prepared as described in Preparation 7) and DIPEA (4.6 mL, 26.45 mmol) were added. The resulting mixture was stirred at room temperature for 2 hours and then diluted with 100 mL of DCM and washed with saturated sodium bicarbonate (150 mL) and brine (150 mL). The organic layer was dried over MgSO4, filtered and concentrated to provide 2.3 g of the title intermediate (92% yield), which was suitable for use without further purification.

Quelle

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