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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1397897생성일: 2026년 10월 25일

4-(Pyridin-2-yl)-1,3-thiazol-2-amine → 4-(3,4-dihydro-2H-quinolin-1-ylsulfonyl)-N-(4-pyridin-2-yl-1,3-thiazol-2-yl)benzamide

https://huagongshe.com/reaction/1397897

반응식

참여 물질

역할이름HCID투입량
반응물4-(Pyridin-2-yl)-1,3-thiazol-2-amineHCID 1092459—
반응물4-(1,2,3,4-Tetrahydroquinoline-1-sulfonyl)benzoic acidHCID 2318939—
생성물4-(3,4-dihydro-2H-quinolin-1-ylsulfonyl)-N-(4-pyridin-2-yl-1,3-thiazol-2-yl)benzamideHCID 3686634—

반응 단계

4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)benzoic acid (1) (400 mg, 1.26 mmol) was treated with 4-(pyridin-2-yl)thiazol-2-amine (290 mg, 1.64 mmol) using method C. The residue was purified using flash chromatography eluting with 50-100% EtOAc in hexanes to give 4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)-N-(4-(pyridin-2-yl)thiazol-2-yl)benzamide as an off-white solid. Yield: 235 mg (39%). 1H-NMR: 8.63-8.60 (m, 1H), 8.21 (d, J=8.5 Hz, 2H), 8.00 (d, J=8.0 Hz, 7.93-7.88 (m, 2H), 7.76 (d, J=8.5 Hz, 2H), 7.61 (d, J=8.0 Hz, 1H), 7.35 (ddd, J=7.5, 5.0, 1.0 Hz, 1H), 7.24-7.19 (m, 1H), 7.14-7.08 (m, 2H), 3.84-3.79 (m, 2H), 2.93 (t, J=8.5 Hz, 2H). 2.45 (t, J=6.5 Hz, 2H), 1.66-1.58 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08901306B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-f3d7d565e979468cb81c0fb051f57146
출처 메모uspto-grants-2014_12