Triphenylphosphine Oxide → 5-chloro-N-[2-(4,5-dihydro-1,3-thiazol-2-yl)-1H-indol-7-yl]thiophene-2-sulfonamide

To a solution of triphenylphosphine oxide (3.57 g) in dichloromethane (20 mL) was slowly added trifluoromethanesulfonic anhydride (1.10 mL) at 0° C. The mixture was stirred for 10 min, and 7-{[(5-chloro-2-thienyl)sulfonyl]amino}-N-[2-(tritylthio)ethyl]-1H-indole-2-carboxamide (1.41 g) was added. The reaction mixture was stirred at room temperature for 3 hr and concentrated. Saturated aqueous sodium hydrogen carbonate was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography and the title compound (0.32 g, yield 37%) was obtained as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:20→1:1, volume ratio). melting point>210° C. (decomposition).

1. customat 0° C
2. stirringThe reaction mixture was stirred at room temperature for 3 hr
3. concentrationconcentrated
4. additionSaturated aqueous sodium hydrogen carbonate was added
5. extractionthe mixture was extracted with ethyl acetate
6. washThe ethyl acetate layer was washed with saturated brine
7. dry with materialdried (MgSO4)
8. concentrationconcentrated

ORD 기록

ord-faa7e714956c4eecb2a05f8bd8ec325b

출처 데이터셋

uspto-grants-2015_02

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08957070B2