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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1397901생성일: 2026년 10월 26일

N-(4-(2-Amino-1,3-thiazol-4-yl)phenyl)acetamide → N-(4-(4-acetamidophenyl)thiazol-2-yl)-4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)benzamide

https://huagongshe.com/reaction/1397901

반응식

참여 물질

역할이름HCID투입량
반응물N-(4-(2-Amino-1,3-thiazol-4-yl)phenyl)acetamideHCID 519881—
반응물4-(1,2,3,4-Tetrahydroquinoline-1-sulfonyl)benzoic acidHCID 2318939—
생성물N-(4-(4-acetamidophenyl)thiazol-2-yl)-4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)benzamideHCID 46912679—

반응 단계

4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)benzoic acid (1) (100 mg, 0.32 mmol) was treated with N-(4-(2-aminothiazol-4-yl)phenyl)acetamide (57 mg, 0.24 mmol) using method B. The residue was purified using flash chromatography eluting with 0-60% EtOAc in hexanes to give N-(4-(4-acetamidophenyl)thiazol-2-yl)-4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)benzamide as a white solid. Yield: 28 mg (22%). 1H-NMR: 10.02 (s, 1H), 8.20 (d, J=8.5 Hz, 2H), 7.86 (d, J=8.5 Hz, 2H), 7.75 (d, J=8.5 Hz, 2H), 7.67-7.58 (m, 4H), 7.24-7.18 (m, 1H), 7.14-7.08 (m, 2H), 3.84-3.80 (m, 2H), 2.45 (t, J=7.0 Hz, 2H), 2.06 (s, 3H), 1.66-1.59 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08901306B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-e35d2b23e4de4d2c820f901b24ce7565
출처 메모uspto-grants-2014_12