돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 630035생성일: 2026년 10월 25일

Triethylamine → HCID 178429519, 화합물

https://huagongshe.com/reaction/630035

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-(Bromomethyl)-1-methyl-1H-benzimidazole hydrobromideHCID 24229451—
반응물HCID 178429541HCID 178429541—
용매EthanolHCID 702—
생성물HCID 178429519HCID 17842951990%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315521B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-ec636c2586ba4316b0e025f379a5eae4
출처 메모uspto-grants-2016_04