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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45393생성일: 2026년 10월 25일

Diisopropylethylamine → N-benzyl-2-(4-benzylbenzamido)-4-methylthiazole-5-carboxamide

https://huagongshe.com/reaction/45393

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Benzylbenzoic acidHCID 136429—
반응물N-Benzyl-2-imino-4-methyl-2,3-dihydro-1,3-thiazole-5-carboximidic acidHCID 210824—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DichloromethaneHCID 6344—
생성물N-benzyl-2-(4-benzylbenzamido)-4-methylthiazole-5-carboxamideHCID 593696733.1%

반응 단계

To a solution of 2-amino-4-methyl-thiazole-5-carboxylic acid benzylamide (0.054 g, 0.22 mmol) and diisopropylethylamine (0.40 mL, 2.3 mmol) in dichloromethane (5 mL) was added 4-benzylbenzoic acid (0.057 g, 0.27 mmol), followed by the addition of N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (0.11 g, 0.28 mmol). The reaction was stirred at ambient temperature over 18 h then concentrated in vacuo. The crude product was purified by preparative HPLC (acetone/water gradient) to afford the title compound (0.003 g); MS (ES+) m/z 442 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541457B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-aac9ba002ade4956bd8a294454f824c1
출처 메모uspto-grants-2013_09