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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78498생성일: 2026년 10월 25일

Dimethylformamide → HCID 178456234, 화합물

https://huagongshe.com/reaction/78498

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Allyl bromideHCID 7841—
반응물Potassium tert-butoxideHCID 23665647—
반응물n-(5-Tert-butylthiazol-2-yl)-5-chloro-2-methoxybenzamideHCID 87094486—
용매TetrahydrofuranHCID 8028—
생성물HCID 178456234HCID 178456234—

반응 조건

온도65 °C

반응 단계

To a solution of Example 244A (410 mg, 1.3 mmol) in 5 mL of tetrahydrofuran:N,N-dimethylformamide (4/1) at 0° C. was added potassium tert-butoxide (230 mg, 1.9 mmol). The reaction mixture was stirred for 1 hour then allyl bromide (0.16 mL, 1.9 mmol) was added. The mixture was warmed to 65° C. and stirred overnight. The mixture was cooled to ambient temperature, concentrated, diluted with CH2Cl2 and washed with water and brine. The organic layer was dried over magnesium sulfate, filtered, and concentrated under reduced pressure. Purification by chromatography (20-50% ethyl ccetate/hexane gradient) afforded the title compound. 1H NMR (CDCl3, 300 MHz) δ ppm 1.34 (s, 9H), 3.90 (s, 3H), 4.78-4.85 (m, 3H), 5.22-5.36 (m, 2H), 5.90-6.09 (m, J=17.0, 10.17 Hz, 1H), 6.62 (s, 1H), 6.90 (d, J=9.2 Hz, 1H), 7.32 (dd, J=8.8, 3.1 Hz, 1H), 8.00 (d, J=2.7 Hz, 1H); MS (DCI/NH3) m/z 365 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841334B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d3cd82d018ef49379c04b7d341157a9b
출처 메모uspto-grants-2014_09