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HRID 1435735생성일: 2026년 10월 27일

4-Bromoaniline → (4-Bromo-phenyl)-[4-chloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazin-2-YL]-amine

https://huagongshe.com/reaction/1435735

반응식

참여 물질

역할이름HCID투입량
반응물4-BromoanilineHCID 7807—
반응물TetrahydrofuranHCID 8028—
반응물DiisopropylethylamineHCID 81531—
반응물2,4-Dichloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazineHCID 85827032—
용매DichloromethaneHCID 6344—
생성물(4-Bromo-phenyl)-[4-chloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazin-2-YL]-amineHCID 1017973086%

반응 단계

A mixture of 2,4-dichloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazine (2.5 g, 9.1 mmol), 4-bromoaniline (1.6 g, 9.3 mmol), tetrahydrofuran (60 ml), and diisopropylethylamine (1.6 ml, 9.2 mmol) was stirred for 1 hour. The solution was treated with dichloromethane (200 ml), washed with saturated aqueous sodium chloride solution (50 ml), and concentrated under reduced pressure. The residual solid was treated with hydrochloric acid (1 M, 25 ml) and stirred vigorously for 30 minutes. Filtration and drying under reduced pressure provided the title compound (3.2 g, 86% yield). 1H NMR (DMSO-d6) 10.75-10.80 (m, 1H), 7.85-7.92 (m, 1H), 7.50-7.65 (m, 4H), 7.40 (m, 1H), 2.58 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07618968B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-478b19e2f94f4a4bb0324881034c6054
출처 메모uspto-grants-2009_11