Reaktion #603648

ord-410b66b9e03742bdb920b2c196790c3d

Reaktionsgleichung

COc1cc(C(=O)O)on1
3-Methoxyisoxazole-5-carboxylic acid
CCO
EtOH
[Li+].[OH-]
LiOH
O
water
CN(C)C(On1nnc2ccc(Cl)cc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HCTU
CCN(C(C)C)C(C)C
DIPEA
CCOC(=O)[C@H](O)C[C@H](N)Cc1ccc(-c2cccc(Cl)c2)cc1
(2R,4R)-4-amino-5-(3′-chlorobiphenyl-4-yl)-2-hydroxypentanoic acid ethyl ester
COc1cc(C(=O)N[C@H](Cc2ccc(-c3cccc(Cl)c3)cc2)C[C@@H](O)C(=O)O)on1
title compound
COc1cc(C(=O)N[C@H](Cc2ccc(-c3cccc(Cl)c3)cc2)C[C@@H](O)C(=O)O)on1
(2R,4R)-5-(3′-Chlorobiphenyl-4-yl)-2-hydroxy-4-[(3-methoxyisoxazole-5-carbonyl)amino]pentanoic Acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe resulting mixture was stirred at room temperature overnight
  2. 2
    workup.STIRRINGThe mixture was stirred at room temperature for 1 hour
  3. 3
    Sonstigeevaporated under reduced pressure
  4. 4
    Sonstigepurified by preparative HPLC

Vorschrift

3-Methoxyisoxazole-5-carboxylic acid (39.4 mg, 275 μmol) and HCTU (128 mg, 310 μmol) were combined in DMF, and stirred for 10 minutes at room temperature. DIPEA (72 μL, 413 μmol) and (2R,4R)-4-amino-5-(3′-chlorobiphenyl-4-yl)-2-hydroxypentanoic acid ethyl ester (50 mg, 0.1 mmol) were added, and the resulting mixture was stirred at room temperature overnight. The mixture was combined with EtOH (402 μL, 6.9 mmol) and 1 M LiOH in water (1.1 mL, 1.1 mmol). The mixture was stirred at room temperature for 1 hour, evaporated under reduced pressure, and purified by preparative HPLC to yield the title compound. MS m/z [M+H]+ calc'd for C22H21ClN2O6, 445.11. found 445.2.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09108934B2uspto-grants-2015_08