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HRID 508635作成日:2026年10月25日

D-Pyroglutamic acid → (R)-N-((1-(5-oxopyrrolidine-2-carbonyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamide

https://huagongshe.com/reaction/508635

反応式

関与物質

役割名称HCID仕込み量
反応物D-Pyroglutamic acidHCID 439685—
反応物Sodium BicarbonateHCID 516892—
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-(piperidin-4-ylmethyl)-3,5-bis(trifluoromethyl)benzamideHCID 57993323—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物(R)-N-((1-(5-oxopyrrolidine-2-carbonyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamideHCID 57993336—

反応条件

温度-20 °C

反応手順

A solution of N-(piperidin-4-ylmethyl)-3,5-bis(trifluoromethyl)benzamide (48 mg, 0.14 mmol), TEA (95 μL, 0.68 mmol), and (R)-5-oxopyrrolidine-2-carboxylic acid (20.66 mg, 0.16 mmol) in DMF (1.5 mL) was treated with a solution of HATU (77 mg, 0.20 mmol) in DMF (1 mL). The reaction mixture was stirred overnight then transferred to a test tube containing saturated aqueous NaHCO3 (4 mL) and EtOAc (4 mL). The biphasic mixture was mixed vigorously and allowed to separate for 15 min. After separation, the mixture was cooled to −20° C. until the aqueous layer was frozen. The organic layer was then poured off and the solvent was removed in vacuo at 50° C. The resulting residue was dissolved in CH2Cl2 (1 mL) and treated with 2M HCl in Et2O (3 mL) and allowed to stir overnight at room temperature. The solvent was removed under reduced pressure and the crude solid was purified by HiTOPs.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096522B2
出典データセットuspto-grants-2015_08
ORD IDord-c0bf54677e164a3a9873009a2342a3bd
出典メモuspto-grants-2015_08