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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12200생성일: 2026년 10월 24일

Water → N-(6-chloro-7-methylsulfanyl-9H-beta-carbolin-8-yl)-2-methyl-nicotinamide

https://huagongshe.com/ko/reaction/12200

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Methylnicotinic acidHCID 643373—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물6-chloro-7-methylsulfanyl-9H-beta-carbolin-8-ylamineHCID 67166635—
용매MethanolHCID 887—
용매PyridineHCID 1049—
생성물N-(6-chloro-7-methylsulfanyl-9H-beta-carbolin-8-yl)-2-methyl-nicotinamideHCID 1136107789.5%

반응 조건

온도100 °C

반응 단계

A 250 ml round-bottom flask with magnetic stirrer was charged with 6-chloro-7-methylsulfanyl-9H-β-carbolin-8-ylamine (Intermediate 28, 2.336 g, 8.86 mmol) and 2-methylnicotinic acid (3.219 g, 23.4 mmol) in 80 ml anhydrous pyridine. To the resulting reaction mixture at RT was added solid 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (7.080 g, 36.9 mmol) and the reaction mixture was heated to 100° C. (oil bath) for 2 days. The resulting mixture was cooled to RT and concentrated (rotavap) to afford a brown residue. The residue was redissolved in MeOH (50 ml), slowly added to a stirring mixture of 5:1 H2O/saturated aqueous sodium bicarbonate (600 mlL) and stirred at RT for ˜18 hr. The precipitated solid was collected via suction filtration, washed with Et2O (2×150 ml), and air-dried to afford 3.036 g of crude N-(6-chloro-7-methylsulfanyl-9H-β-carbolin-8-yl)-2-methyl-nicotinamide as a brown solid. The crude material was purified via HPLC (yields=˜40-60%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727985B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-fe7796a45668470a88b977caac4dbba7
출처 메모uspto-grants-2010_06