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HRID 14035Erstellt: 24. Oktober 2026

Methanol → Methyl 4'-[(dimethylamino)sulfonyl)-5-[(dipropylamino)carbonyl][1,1'-biphenyl]-3-carboxylic acid

https://huagongshe.com/de/reaction/14035

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktMethyl 4'-[(dimethylamino)sulfonyl]-5-[(dipropylamino)carbonyl)[1,1'-biphenyl]-3-carboxylateHCID 69680482—
LösungsmittelWaterHCID 962—
LösungsmittelSodium HydroxideHCID 14798—
ProduktMethyl 4'-[(dimethylamino)sulfonyl)-5-[(dipropylamino)carbonyl][1,1'-biphenyl]-3-carboxylic acidHCID 21094805—

Reaktionsbedingungen

Temperatur22.5 °C

Reaktionsschritte

A mixture of methyl 4′-[(dimethylamino)sulfonyl]-5-[(dipropylamino)carbonyl][1,1′-biphenyl]-3-carboxylate (XXXVIII, step 2, 555 mg, 1.24 mmol) in methanol (6 mL) and sodium hydroxide (2 mL of a 6.0 M mixture in water, 12 mmol) is stirred at 20-25 degrees C. for 4 hours. The reaction mixture is partitioned between ethyl acetate (40 mL) and water (40 mL). The aqueous phase is acidified to pH=4 with hydrochloric acid (1N), extracted with ether (3×100 mL), and the combined organic phases are concentrated under reduced pressure to give methyl 4′-[(dimethylamino)sulfonyl]-5-[(dipropylamino)carbonyl][1,1′-biphenyl]-3-carboxylic acid (IX-XXXIX), NMR (300 MHz, CDCl3): δ 8.37, 8.12, 7.89, 7.80, 3.51, 3.22, 2.76, 1.74, 1.59, 1.02 and 0.79.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727997B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-9b3286a75e7f49f1a4b625407d9b2352
Quellennotizuspto-grants-2010_06