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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15028생성일: 2026년 10월 23일

4-(Morpholin-4-yl)benzoic acid → 6-(4-Morpholinophenyl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

https://huagongshe.com/ko/reaction/15028

반응식

참여 물질

역할이름HCID투입량
반응물4-(Morpholin-4-yl)benzoic acidHCID 345278—
반응물HCID 178488244HCID 178488244—
용매Phosphorus oxychlorideHCID 24813—
생성물6-(4-Morpholinophenyl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazoleHCID 2495522824.4%

반응 단계

A mixture of 4-morpholinobenzoic acid (86 mg, 0.42 mmol) and 4-amino-3-mercapto-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazole (102 mg, 0.36 mmol) was refluxed in POCl3 (5 mL) for 2 h. The reaction mixture was cooled to room temperature and excess POCl3 was removed under vacuum. The residue was dissolved in ethyl acetate and washed with saturated NaHCO3. The organic layer was dried over anhydrous Na2SO4, filtered and concentrated. The crude product was purified by chromatography (80% ethyl acetate/hexane; 1 mL methanol/100 mL of solvent) to give the title compound as a yellow solid (40 mg, 0.088 mmol, 24%). 1H NMR (CDCl3): 7.78 (m, 2H), 7.73 (s, 2H), 6.98 (m, 2H), 4.00 (s, 6H), 3.94 (s, 3H), 3.89 (m, 4H), 3.41 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732468B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1a99ddf1b32949a193135c68e1c70694
출처 메모uspto-grants-2010_06