Dimethylacetamide → N-{2-[5-(hydroxymethyl)-1,3-thiazol-2-yl]-1H-indol-7-yl}-N-methylthiophene-2-sulfonamide

Temperatur

80 °C

A mixture of 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide (1.00 g), bromomalonaldehyde (0.86 g) and N,N-dimethylacetamide (8 ml) was stirred at 80° C. for 3 hr. Water was added to the reaction mixture, and the resulting crystals were collected by filtration, washed with water, and dried. The obtained crystals were dissolved in tetrahydrofuran (8 ml) and methanol (8 ml), sodium borohydride (63 mg) was added at 0° C., and the mixture was stirred at 0° C. for 1 hr. The reaction mixture was concentrated, 10% aqueous citric acid solution was added, and the resulting crystals were collected by filtration, washed with water, and dried. The crystals were subjected to silica gel column chromatography to give the title compound (0.43 g, yield 39%) as colorless crystals from a fraction eluted with ethyl acetate-hexane (3:1, volume ratio). melting point 201-202° C.

1. filtrationthe resulting crystals were collected by filtration
2. washwashed with water
3. customdried
4. dissolutionThe obtained crystals were dissolved in tetrahydrofuran (8 ml)
5. additionmethanol (8 ml), sodium borohydride (63 mg) was added at 0° C.
6. stirringthe mixture was stirred at 0° C. for 1 hr
7. concentrationThe reaction mixture was concentrated
8. addition10% aqueous citric acid solution was added
9. filtrationthe resulting crystals were collected by filtration
10. washwashed with water
11. customdried

ORD-Eintrag

ord-7a221e9922ac4575a9792a55f9f95e0f

Quelldatensatz

uspto-grants-2013_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08410087B2