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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33576생성일: 2026년 10월 24일

1-Naphthaleneboronic acid → 5-Methyl-4-naphthalen-1-yl-oxazol-2-ylamine

https://huagongshe.com/ko/reaction/33576

반응식

참여 물질

역할이름HCID투입량
반응물1-Naphthaleneboronic acidHCID 254532—
반응물Potassium AcetateHCID 517044—
반응물Trifluoro-methanesulfonic acid 2-tert-butoxycarbonylamino-5-methyl-oxazol-4-yl esterHCID 86590770—
용매1,4-DioxaneHCID 31275—
생성물5-Methyl-4-naphthalen-1-yl-oxazol-2-ylamineHCID 5979682614%

반응 조건

온도180 °C

반응 단계

A mixture of trifluoro-methanesulfonic acid 2-tert-butoxycarbonylamino-5-methyl-oxazol-4-yl ester (100 mg), 1-naphthaleneboronic acid (61 mg) palladium (0) tetrakis(triphenylphosphine) (17 mg), potassium acetate (85 mg) and 1,4-dioxane (5 mL) was heated at 180° C. for 24 hours. The solvent was removed under reduced pressure and to the resulting yellow oil was added dichloromethane (18 mL) and trifluoroacetic acid (2 mL). The mixture was stirred at room temperature for 1 hour and then the solvent was removed under reduced pressure, the resulting oil was diluted with ethyl acetate and washed with a saturated solution of sodium hydrogen carbonate, brine, dried over magnesium sulfate, filtered and the solvent removed under reduced pressure to afford a brown oil. Purification by column chromatography afforded 5-methyl-4-naphthalen-1-yl-oxazol-2-ylamine (30) (9 mg, 14%) as a white solid. 1H NMR (DMSO-D6): 2.15 (3H, s), 6.5 (2H, br s), 7.4-7.5 (4H, m), 7.85-7.90 (2H, m), 8.2 (1H, m). Mass Spectrum (m/z): 225 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429607B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-82babac5748d4d23880cd6ea35080aee
출처 메모uspto-grants-2008_09