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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45321생성일: 2026년 10월 24일

Benzylamine → N-(5-Benzylcarbamoyl-4-methylthiazol-2-yl)isonicotinamide

https://huagongshe.com/ko/reaction/45321

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물4-MethylmorpholineHCID 7972—
반응물2-Chloro-4,6-dimethoxy-1,3,5-triazineHCID 18450—
반응물4-Methyl-2-[(pyridine-4-carbonyl)amino]thiazole-5-carboxylic acidHCID 82226332—
용매TetrahydrofuranHCID 8028—
생성물N-(5-Benzylcarbamoyl-4-methylthiazol-2-yl)isonicotinamideHCID 146826145%

반응 단계

To a mixture of 4-methyl-2-[(pyridine-4-carbonyl)amino]thiazole-5-carboxylic acid (0.40 g, 1.50 mmol) and 4-methylmorpholine (0.25 mL, 2.20 mmol) in tetrahydrofuran (50 mL) was added 2-chloro-4,6-dimethoxy-1,3,5-triazine (0.32 g, 1.80 mmol). The resulting mixture was stirred at ambient temperature for 4 h, and then benzylamine (0.2 mL, 1.80 mmol) was added. The reaction mixture was stirred at room temperature for 47 h and then concentrated. Purification of the residue by column chromatography afforded the title compound in 45% yield (0.24 g); m.p. 171-172° C.; 1H NMR (DMSO-d6, 300 MHz) δ 13.15 (s, 1H), 8.78-8.63 (m, 3H), 7.94 (dd, J=1.5, 4.5 Hz, 2H), 7.32-7.17 (m, 5H), 4.38 (d, J=6.0 Hz, 2H), 2.51 (s, 3H); 13C NMR (DMSO-d6, 75 MHz) δ 162.0, 150.9, 140.0, 139.5, 128.7, 127.7, 127.2, 122.2, 114.3, 43.1, 17.1; MS (ES+) m/z 353.3 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541457B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-beef577cf9ab4363be504d74db41d874
출처 메모uspto-grants-2013_09