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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14178생성일: 2026년 10월 23일

Oxazole → 1-butyl-4-(1,3-oxazol-2-yl)-1H-indole-6-carboxylic acid

https://huagongshe.com/ko/reaction/14178

반응식

참여 물질

역할이름HCID투입량
반응물OxazoleHCID 9255—
반응물Methyl 1-butyl-4-iodo-1H-indole-6-carboxylateHCID 21086136—
촉매ZincchlorideHCID 3007855—
용매TetrahydrofuranHCID 8028—
생성물1-butyl-4-(1,3-oxazol-2-yl)-1H-indole-6-carboxylic acidHCID 2108516970.4%

반응 조건

온도85 °C

반응 단계

To a −72° C. solution of oxazole (0.069 g) in dry THF (20 mL) was added dropwise 1.6 M N-butyl lithium (0.68 mL). The mixture was stirred at −72° C. for 30 minutes at which time 1.0 M zinc chloride (3.3 mL) was added. The mixture was allowed to warm to 0° C. at which time methyl 1-butyl-4-iodo-1H-indole-6-carboxylate (0.37 g) and tetrakis triphenylphosphine palladium(0) (0.07 g) were added and the mixture heated to 85° C. The mixture was heated at 85° C. for 20 h then cooled to room temperature and partitioned between water and ethyl acetate. The layers were separated and the organic layer washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Column chromatography was performed on silica gel (100 mL) using 20% ethyl acetate in hexanes as eluent. The residue was dissolved in methanol (10 mL) and 1N NaOH (3 mL) and heated at 60° C. for 2 h. The mixture was acidified to pH 4 with 1N HCl and extracted with ethyl acetate. The ethyl acetate extracts were dried over anhydrous sodium sulfate and concentrated to dryness under reduced pressure to give 0.2 g of the title compound: MS (ESI+) for C16H16N2O3 m/a 283.16 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9220c86cc2df47d9b0a7723b3c4ed323
출처 메모uspto-grants-2010_06