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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 471023생성일: 2026년 10월 26일

Trifluoroacetic acid → 1-Oxa-4,9-diazaspiro[5,5]undecan-4-yl(2-(trifluoromethyl)thiazol-4-yl)methanone trifluoroacetate

https://huagongshe.com/reaction/471023

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참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물2-(Trifluoromethyl)-1,3-thiazole-4-carboxylic acidHCID 28875557—
반응물Tert-butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochlorideHCID 66964240—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물1-Oxa-4,9-diazaspiro[5,5]undecan-4-yl(2-(trifluoromethyl)thiazol-4-yl)methanone trifluoroacetateHCID 86636751—

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온도0 °C

반응 단계

A solution of tert-butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochloride (WuXi PharmaTech) (0.594 g) and 2-(trifluoromethyl)thiazole-4-carboxylic acid (0.4 g) in DMF (10 mL) was treated with triethylamine (0.848 mL) and cooled to 0° C. HATU (1.003 g) was added and the mixture stirred at 20° C. for 2 hours. The mixture was partitioned between ethyl acetate and brine, the organic layer was washed twice with brine, dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure. The crude product was purified by flash silica chromatography eluting with 40% ethyl acetate in isohexane to yield the product as the free base. This was dissolved in dichloromethane (40 mL) and treated with trifluoroacetic acid (10 mL) and then the mixture was allowed to stand at 20° C. for 1 hour. Toluene (60 mL) was added and the solvent removed under reduced pressure to afford the subtitled compound. Yield 0.740 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629271B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-31ae822026264ea3a9333456986c7e23
출처 메모uspto-grants-2014_01