돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38429생성일: 2026년 10월 24일

Guanidine → 2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile

https://huagongshe.com/ko/reaction/38429

반응식

참여 물질

역할이름HCID투입량
반응물GuanidineHCID 3520—
반응물Guanidine HydrochlorideHCID 5742—
반응물Benzenamine hydrochloride (1:1)HCID 8870—
반응물Sodium MethoxideHCID 10942334—
반응물3,3-Bis-dimethylamino-2-(4-ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-propionitrileHCID 59598706—
용매EthanolHCID 702—
생성물2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrileHCID 6705341355%

반응 단계

3,3-Bis-dimethylamino-2-(4-ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-propionitrile (590 mg, 2 mmol) and aniline HCl (1.1 g, 9 mmol) in 5 mL absolute ethanol were heated at reflux for 2.0 hours. In a separate flask, guanidine HCl (0.850 mg., 9 mmol) and sodium methoxide solution (1.83 ml, 9 mmol, 4.9 molar solution in methanol) were mixed in 1 ml Ethanol. The guanidine solution was added to the reaction mixture via pipette, and the reaction mixture was heated to reflux for 5 hours, then cooled. Solvent was removed in vacuo, and the residue was, chromatographed (5% MeOH/methylene chloride/1% Na4OH) to give 368 mg 2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile, 61%. Also present was 50 mg of 5-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-pyrimidine-2,4-diamine, 9%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524725B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-cc4c99025821491089fd53ccd157da18
출처 메모uspto-grants-2013_09