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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14171생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/14171

반응식

참여 물질

역할이름HCID투입량
반응물Butyl iodideHCID 10962—
반응물Potassium HydroxideHCID 14797—
반응물methyl 4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylateHCID 21086207—
용매DimethylformamideHCID 6228—
생성물1-Butyl-4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylic acidHCID 21085174—

반응 조건

온도70 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a947873d89804a60ae57d2f24f7a0ae0
출처 메모uspto-grants-2010_06