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HRID 401769作成日:2026年10月26日

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

https://huagongshe.com/reaction/401769

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2,4-DimethoxybenzaldehydeHCID 69175—
反応物Sodium borohydrideHCID 4311764—
反応物1,2,4-Thiadiazol-3-amineHCID 20249664—
触媒PiperidineHCID 8082—
触媒ChlorotitaniumtriisopropoxideHCID 11673339—
溶媒DichloromethaneHCID 6344—
溶媒HeptaneHCID 8900—
溶媒Sodium BicarbonateHCID 516892—
生成物N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amineHCID 5773221618.3%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741934B2
出典データセットuspto-grants-2014_06
ORD IDord-d6b78093d9ed4b27b68df90c6a4b3775
出典メモuspto-grants-2014_06