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HRID 576994作成日:2026年10月26日

Triethylamine → HCID 178429519、化合物

https://huagongshe.com/reaction/576994

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-(Bromomethyl)-1-methyl-1H-benzimidazole hydrobromideHCID 24229451—
反応物HCID 178429541HCID 178429541—
溶媒EthanolHCID 702—
生成物HCID 178429519HCID 17842951990%

反応手順

A mixture of 2-(bromomethyl)-1-methyl-benzimidazole hydrobromide (6.8 mmol), 6-methyl-2-sulfanylpyrimidin-4-ol (740 mg, 5.2 mmol), and triethylamine (4 mL, 28.7 mmol) in absolute ethanol (30 mL) was stirred at room temperature overnight. The mixture was recovered, evaporated, and then co-evaporated with EtOAc (20 mL). The solid residue was treated with water (200 mL). The solid product was recovered by filtration, washed with water (2×20 mL), diethyl ether (2×20 mL), and hexanes (2×20 mL), and then dried in vacuo, affording 6-methyl-2-{[(1-methyl-1H-benzimidazol-2-yl)methyl]sulfanyl}pyrimidin-4-ol (1.3 g, 90% yield); 1H NMR (400 MHz, DMSO-d6): δ 2.18 (s, 3H), 3.83 (s, 3H), 4.70 (s, 2H), 6.02 (s, 1H), 7.19 (m, 2H), 7.53 (m, 2H); M+ 287. The product was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040538B2
出典データセットuspto-grants-2015_05
ORD IDord-d81ca144a97f4585b75f90a410418912
出典メモuspto-grants-2015_05