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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 254665생성일: 2026년 10월 25일

Hydrochloric Acid → HCID 178490665, 화합물

https://huagongshe.com/reaction/254665

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-(Chloromethyl)-1,3-thiazoleHCID 2763290—
반응물Potassium tert-butoxideHCID 23665647—
반응물n-(5-Tert-butylthiazol-2-yl)-5-chloro-2-methoxybenzamideHCID 87094486—
촉매Tetrabutylammonium IodideHCID 67553—
용매Ethyl AcetateHCID 8857—
용매tetrahydrofuran N,N-dimethylformamideHCID 21974620—
생성물HCID 178490665HCID 178490665—

반응 조건

온도80 °C

반응 단계

To a solution of Example 74B (0.75 g, 2.31 mmol) in DMF/THF (1:4, 20 mL) were added potassium tert-butoxide (0.77 g, 6.93 mmol), tetrabutylammonium iodide (0.09, 0.23 mmol) and the commercially available HCl salt of 4-(chloromethyl)thiazole (TCI-US, 0.59 g, 3.46 mmol). The reaction mixture was stirred at 80° C. for 16 hours, cooled, diluted with ethyl acetate (20 mL) and quenched with saturated aqueous NaHCO3 (20 mL). The aqueous layer was extracted with ethyl acetate (2×20 mL). The combined organic layers were washed with water (1×25 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography using an Analogix® Intelliflash280 ™ (SiO2, 0-100% ethyl acetate in hexanes) to afford the title compound. 1H NMR (300 MHz, dimethylsulfoxide-d6) δ ppm 1.32 (s, 9H), 3.76 (s, 3H), 5.49 (s, 2H), 7.09 (d, J=9.2 Hz, 1H), 7.36 (s, 1H), 7.44 (dd, J=9.0, 2.9 Hz, 1H), 7.57 (d, J=2.0 Hz, 1H), 7.61 (d, J=3.1 Hz, 1H), 9.10 (d, J=2.0 Hz, 1H); MS (ESI+) m/z 422 (M+H)+; Anal. Calculated for C19H20ClN3O2S2: C, 54.08; H, 4.78; N, 9.96. Found: C, 54.10; H, 4.62; N, 9.81.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875640B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-73c460a7e32349f69ad9b0c6e1420ee6
출처 메모uspto-grants-2011_01