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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219549생성일: 2026년 10월 23일

Pyridine → n-[4-(Thiazol-2-ylsulfamoyl)-phenyl]-2-(8-trifluoromethyl-quinolin-4-yloxy)-acetamide

https://huagongshe.com/ko/reaction/219549

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물SulfathiazoleHCID 5340—
반응물Oxalyl chlorideHCID 65578—
반응물2-((8-(Trifluoromethyl)quinolin-4-yl)oxy)acetic acidHCID 53420975—
용매DichloromethaneHCID 6344—
생성물n-[4-(Thiazol-2-ylsulfamoyl)-phenyl]-2-(8-trifluoromethyl-quinolin-4-yloxy)-acetamideHCID 5793644069.5%

반응 조건

온도0 °C

반응 단계

(8-Trifluoromethylquinolin-4-yloxy)-acetic acid (0.50 g, 1.84 mmol) was suspended in 20 mL DCM with rapid stirring. At rt, oxalyl chloride (0.19 mL, 1.2 equiv) was added dropwise and stirring continued for 4 h. Solvent and excess oxalyl chloride were removed in vacuo, the white residue was re-suspended in DCM, and the mixture cooled to 0° C. N′-(2-thiazolyl)sulfanilamide (0.47 g, 1.0 equiv) was added followed by pyridine (0.30 mL, 2.0 equiv). The mixture was allowed to warm to rt overnight. The solid was collected and rinsed with fresh DCM. Further purification was effected by suspending the solid in 20 mL methanol, stirring vigorously for 4 h, and filtration. After drying under vacuum, white solid 0.65 g (69%) was obtained. 1H-NMR (DMSO-d6) 5.11 (s, 2H), 6.79 (d, J=4.8 Hz, 1H), 7.12 (d, J=5.2 Hz, 1H), 7.22 (d, J=4.8 Hz, 1H), 7.71 (t, J=8.0 Hz, 1H), 8.17 (d, J=8.0 Hz, 1H), 8.55 (d, J=8.0 Hz, 1H), 8.85 (d, J=5.2 Hz, 1H); 13C-NMR (DMSO-d6) 68.0, 103.6, 108.8, 120.0, 122.0, 124.8 (q, J=270 Hz), 125.1, 125.4, 126.4 (q, J=33 Hz), 127.7, 127.8, 129.2, 137.7, 142.1, 145.6, 153.2, 161.2, 166.5, 169.4 LC/MS (10-99%) M/Z: M+1 obs=509.5; tR=3.13 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202861B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-9365a5b5bb7c4446b37894b84f0e84da
출처 메모uspto-grants-2012_06