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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 401769생성일: 2026년 10월 24일

Triethylamine → N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amine

https://huagongshe.com/ko/reaction/401769

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,4-DimethoxybenzaldehydeHCID 69175—
반응물Sodium borohydrideHCID 4311764—
반응물1,2,4-Thiadiazol-3-amineHCID 20249664—
촉매PiperidineHCID 8082—
촉매ChlorotitaniumtriisopropoxideHCID 11673339—
용매DichloromethaneHCID 6344—
용매HeptaneHCID 8900—
용매Sodium BicarbonateHCID 516892—
생성물N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amineHCID 5773221618.3%

반응 단계

2,4 Dimethoxybenzaldehyde (4.1 g, 24 mmol, 1 eq), 2 amino-1,2,4-thiadiazole (2.5 g, 24.7 mmol, 1 eq), Et3N (3.04 g, 30 mmol, 1 eq) and piperidine (25 mg, 0.297 mmol, 0.012 eq) were combined in DCM (100 ml) and the reaction mixture heated to reflux over sieves for 72 hours. The reaction mixture was cooled to room temperature and chlorotitaniumisopropoxide (1M solution in hexane, 29.7 ml, 29.7 mmol, 1.2 eq) was added and the reaction mixture stirred at room temperature for 15 minutes. The sieves were removed by filtration and the reaction mixture diluted with MeOH (50 ml). Sodium borohydride (3.7 g, 99 mmol, 4.0 eq) was added portionwise and the reaction mixture stirred for 1 hour. The reaction mixture was diluted with saturated sodium hydrogen carbonate (100 ml) and the resulting titanium precipitate removed by filtration through Celite. The filtrate was dried over sodium sulphate, filtered and evaporated in vacuo. The crude material was purified by column chromatography eluting with 15-60% ethyl acetate: heptane to yield the title compound (1.1 g, 4.38 mmol, 17%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741934B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-d6b78093d9ed4b27b68df90c6a4b3775
출처 메모uspto-grants-2014_06