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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Sulfide | HCID 402 | — |
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | [1-(Pyridin-4-yl)piperidin-4-yl]methanamine | HCID 10607746 | — |
| 반응물 | 3-chloro-N-(4-chlorophenyl)pyridine-4-carboxamide | HCID 12150691 | — |
| 촉매 | copper(I) bromide | HCID 24593 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | N-(4-Chlorophenyl)-2-[1-(4-pyridyl)piperidin-4-ylmethyl]aminopyridine-3-carboxamide | HCID 12990573 | 13% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06710057B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-cf9fc4aa229741c99a6932a90156caab |
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| 출처 메모 | uspto-grants-2004_03 |
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