戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 876341作成日:2026年10月25日

3-Methyl-isonicotinic acid → N-{1-[(3-Methylpyridin-4-yl)carbonyl]-5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzenecarboxamide

https://huagongshe.com/reaction/876341

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-isonicotinic acidHCID 1502003—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物N-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamideHCID 66701397—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物N-{1-[(3-Methylpyridin-4-yl)carbonyl]-5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzenecarboxamideHCID 66762085—

反応手順

38 mg (0.28 mmol) of 3-methylpyridine-4-carboxylic acid together with 131 mg (0.34 mmol) of HATU and 56 mg (0.46 mmol) of 4-dimethylaminopyridine were initially charged in 2 ml of DMF, and 80 mg (0.23 mmol) of N-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamide were added. The reaction mixture was stirred overnight at RT and then purified by preparative HPLC (Reprosil C18, water/acetonitrile gradient). Yield: 65 mg (59% of theory)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08987248B2
出典データセットuspto-grants-2015_03
ORD IDord-cef5649329494c15b9cfb79dcd182636
出典メモuspto-grants-2015_03