Reaktion #48941

ord-d00af014a3574eae896426b144fefafb

Reaktionsgleichung

O=P([O-])(O)O.[K+]
KH2PO4
[H-].[Na+]
Sodium hydride
N[C@H]1CC[C@@H](C(=O)O)CC1
cis-4-amino-1-cyclohexanecarboxylic acid
COc1ccc2c(Cl)cc(=O)oc2c1OC1CCCC1
4-chloro-8-(cyclopentyloxy)-7-methoxy-2H-chromen-2-one
COc1ccc2c(N[C@H]3CC[C@@H](C(=O)O)CC3)cc(=O)oc2c1OC1CCCC1
cis-4-(8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-ylamino)cyclohexanecarboxylic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ethyl acetate
  2. 2
    SonstigeThe extract was dried
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated
  5. 5
    Sonstigepurified by reverse-phase HPLC (30→100% MeCN/H2O)

Vorschrift

Sodium hydride (50 mg, 60%, 1.25 mmol) was added to a solution of cis-4-amino-1-cyclohexanecarboxylic acid (83 mg, 0.580 mmol) and anhydrous DMSO (2 mL) at rt under N2. After 10 min, 4-chloro-8-(cyclopentyloxy)-7-methoxy-2H-chromen-2-one (114 mg, 0.387 mmol, Example 7, Step 1) was added, and the mixture was stirred for 3 d, poured into 1M KH2PO4 and extracted with ethyl acetate. The extract was dried, filtered, concentrated, and purified by reverse-phase HPLC (30→100% MeCN/H2O) to give cis-4-(8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-ylamino)cyclohexanecarboxylic acid: 1H NMR (400 MHz, DMSO-d6): δ 7.85 (d, 1H), 7.10 (d, 1H), 7.01 (d, 1H), 5.10 (s, 1H), 4.81 (m, 1H), 3.87 (s, 3H), 3.50 (m, 1H), 2.56 (m, 1H), 2.04 (m, 2H), 1.79-1.58 (m, 14H); MS (ESI): 402.0.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745646B2uspto-grants-2010_06