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HRID 1754914作成日:2026年10月25日

Diisopropylethylamine → HCID 66817124、化合物

https://huagongshe.com/reaction/1754914

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物2-Fluoro-4-(trifluoromethyl)benzoic acidHCID 518003—
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tert-Butyl 4-amino-4-carbamoylpiperidine-1-carboxylateHCID 10562199—
溶媒DimethylformamideHCID 6228—
生成物HCID 66817124HCID 66817124—

反応手順

HATU (939 mg, 2.47 mmol) and DIPEA (525 μL, 3.09 mmol) were added to a solution of 4-amino-4-carbamoyl-piperidine-1-carboxylic acid tert-butyl ester (500 mg, 2.06 mmol) and 2-fluoro-4-trifluoromethyl-benzoic acid (514 mg, 2.47 mmol) in DMF (10 mL). The mixture was stirred at room temperature for 19 hours and then quenched with a saturated aqueous ammonium chloride solution. The reaction mixture was diluted with EtOAc, and the organic layer was then washed with H2O and saturated brine, dried over MgSO4 and concentrated under reduced pressure. The resulting residue was triturated with n-hexane and EtOAc and then collected by filtration to give 4-carbamoyl-4-(2-fluoro-4-trifluoromethyl-benzoylamino)-piperidine-1-carboxylic acid tert-butyl ester as a white solid. This was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09169254B2
出典データセットuspto-grants-2015_10
ORD IDord-c4df05d6069349b4b43cec6b75c6eb06
出典メモuspto-grants-2015_10