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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45377생성일: 2026년 10월 24일

4-Methylmorpholine → HCID 59369652, 화합물

https://huagongshe.com/ko/reaction/45377

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물BenzoylhydrazineHCID 11955—
반응물Isobutyl chloroformateHCID 62365—
반응물2-Benzoylamino-4-methyl-thiazole-5-carboxylic acidHCID 856802—
용매Ethyl AcetateHCID 8857—
생성물HCID 59369652HCID 5936965214%

반응 단계

To a solution of 2-benzamido-4-methylthiazole-5-carboxylic acid (0.30 g, 1.14 mmol) in tertahydrofuran (28 mL) was added N-methylmorpholine (0.23 mL, 0.21 g, 2.09 mmol) under nitrogen atmosphere, followed by the addition of isobutyl chloroformate (0.2 mL, 0.21 g, 1.54 mmol) dropwise at ambient temperature. The mixture was stirred at ambient temperature for 7 hours. Benzhydrazide (0.23 g, 1.71 mmol) and 4-methylmorpholine (0.15 mL, 0.14 g, 1.36 mmol) were added to the reaction mixture. After being stirred at ambient temperature for 18 hours, the reaction mixture was diluted with ethyl acetate (50 mL), washed with water (3×10 mL). The organic phase was separated and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated in vacuo. The crude product was purified by column chromatography eluted with ethyl acetate/hexanes (20/80 to 30/70) to afford the title compound as a white solid (0.059 g, 14% yield); m.p. 258-260° C.; 1H NMR (DMSO-d6, 300 MHz) δ 12.90 (br, 1H), 10.46 (s, 1H), 10.10 (s, 1H), 8.09 (d, J=7.4 Hz, 2H), 7.93 (d, J=6.9 Hz, 2H), 7.65-7.47 (m, 6H), 2.56 (s, 3H); MS (ES+) m/z 381.4 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541457B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d31cf82d68bb44b7ba94b65dc8ba2bd1
출처 메모uspto-grants-2013_09