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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1469934생성일: 2026년 10월 25일

Triethylamine → N-(5-bromo-1,3-thiazol-2-yl)adamantane-1-carboxamide

https://huagongshe.com/reaction/1469934

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Adamantanecarbonyl chlorideHCID 98915—
반응물5-Bromothiazol-2-amine monohydrobromideHCID 2723848—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물N-(5-bromo-1,3-thiazol-2-yl)adamantane-1-carboxamideHCID 4976064065%

반응 조건

온도80 °C

반응 단계

A mixture of 2-amino-5-bromothiazole monohydrobromide (3.00 g, 11.5 mmol), 1-adamantanecarbonyl chloride (2.74 g, 13.8 mmol), 4-dimethylaminopyridine (1.10 g, 0.90 mmol) and triethylamine (3.20 mL, 23.0 mmol) in 100 mL of THF was stirred at 80° C. for 48 hours. The mixture was cooled to ambient temperature, diluted with 100 mL of ethyl acetate and washed with brine. The layers were separated and the aqueous phase was extracted with 2×50 mL ethyl acetate. The combined organic extracts were dried over anhydrous Na2SO4, filtered, and concentrated. Purification by column chromatography (SiO2, 20% ethyl acetate: 80% hexane) afforded 2.55 g of the title compound. 1H NMR (400 MHz, DMSO-d6) δ 1.67-1.72 (m, 6H) 1.92 (d, J=2.8 Hz, 6H) 1.97-2.04 (m, 3H) 7.55 (s, 1H) 11.50 (br m, 1H); MS (DCI/NH3) m/z 341 (M)+, 343 (M+2)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006275B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-fbc07d08f3aa4060ba559cb17fc0b8cb
출처 메모uspto-grants-2015_04