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HRID 14171Erstellt: 27. Oktober 2026

Butyl iodide → 1-Butyl-4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylic acid

https://huagongshe.com/reaction/14171

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyl iodideHCID 10962—
EduktPotassium HydroxideHCID 14797—
Eduktmethyl 4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylateHCID 21086207—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Butyl-4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylic acidHCID 21085174—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a mixture of methyl 4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylate (0.437 g) in DMF (15 mL) was added potassium hydroxide (0.087 g) and iodobutane (0.34 mL). The mixture was heated to 70° C. for 6 h. then stirred at room temperature for 72 h. The mixture was partitioned between water and ethyl acetate, the layers were separated and the organic layer washed three times with water. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was dissolved in methanol (5 mL) to which was added 1N NaOH (2 mL) and the mixture heated to 50° C. for 1 h. The mixture was cooled to room temperature and poured into water and washed with ether. The aqueous layer was acidified to pH 4 with 1N HCl and the product extracted into ethyl acetate which was dried over anhydrous sodium sulfate, filtered and concentrated to dryness to give 0.377 g of the title compound: 1H NMR (CDCl3) δ 0.973, 1.38, 1.87, 3.01, 3.45, 4.21, 6.71, 7.36, 7.82, 8.18.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727997B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-a947873d89804a60ae57d2f24f7a0ae0
Quellennotizuspto-grants-2010_06