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HRID 645508作成日:2026年10月25日

HOAt → (r)-2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid (2-phenyl 1-pyrrolidin-1-ylmethylethyl)amide

https://huagongshe.com/reaction/645508

反応式

関与物質

役割名称HCID仕込み量
反応物HOAtHCID 181649—
反応物(r)-2-Phenyl-1-pyrrolidin-1-ylmethylethylamineHCID 12184138—
反応物2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acidHCID 68703276—
反応物EDCl H2OHCID 87672115—
溶媒DimethylformamideHCID 6228—
生成物(r)-2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid (2-phenyl 1-pyrrolidin-1-ylmethylethyl)amideHCID 91139520—

反応手順

To a solution of the crude 2-cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid (22 mg, step 74.5) in DMF (1.5 mL) are added (R)-2-phenyl-1-pyrrolidin-1-ylmethylethylamine (0.083 mmol), EDCl—H2O (0.11 mmol), and HOAt (0.11 mmol) at room temperature. The reaction mixture is stirred for 24 h and the reaction is quenched by the addition of H2O. The mixture is extracted with AcOEt, and the organic extracts are dried over Na2SO4, filtered, and concentrated in vacuo. The resulting residue is purified by RP-HPLC to give the title compound; MS (M+1)+: 474, Rf (solvent): 0.63 (CH2Cl2:MeOH=10:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07704996B2
出典データセットuspto-grants-2010_04
ORD IDord-ebbaec1b7fa74d20b57f0e984fa021c0
出典メモuspto-grants-2010_04