돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49849생성일: 2026년 10월 23일

Hydrogen Sulfide → N-(4-Chlorophenyl)-2-[1-(4-pyridyl)piperidin-4-ylmethyl]aminopyridine-3-carboxamide

https://huagongshe.com/ko/reaction/49849

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen SulfideHCID 402—
반응물DimethylformamideHCID 6228—
반응물[1-(Pyridin-4-yl)piperidin-4-yl]methanamineHCID 10607746—
반응물3-chloro-N-(4-chlorophenyl)pyridine-4-carboxamideHCID 12150691—
촉매copper(I) bromideHCID 24593—
용매MethanolHCID 887—
생성물N-(4-Chlorophenyl)-2-[1-(4-pyridyl)piperidin-4-ylmethyl]aminopyridine-3-carboxamideHCID 1299057313%

반응 조건

온도110 °C

반응 단계

A mixture of 3-chloro-N-(4-chlorophenyl)pyridine-4-carboxamide (130 mg, 0.49 mmol), 1-(4-pyridyl)piperidine-4-methylamine (187 mg, 0.98 mmol), and copper(1) bromide (70 mg) in dimethylformamide (1 mL) was heated at 110° C. After 18 h, the mixture was diluted with MeOH, filtered, and concentrated. The residue was treated with 6:1 chloroform:water (10 mL) followed by MeOH until a homogenoeus solution resulted. The solution was treated with hydrogen sulfide(g), heated at reflux for 0.1 h, and filtered through diatomaceous earth. The filtrate was concentrated and the residue taken up in water, 1 N NaOH, and EtOAc. The aqueous layer was washed with EtOAc (3×), the combined extracts were dried (sodium sulfate), filtered and concentrated. The residue was purified by RPHPLC yielding 29 mg (13%) of the title compound as a hydrochloride salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710057B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-cf9fc4aa229741c99a6932a90156caab
출처 메모uspto-grants-2004_03