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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645508생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물HOAtHCID 181649—
반응물(r)-2-Phenyl-1-pyrrolidin-1-ylmethylethylamineHCID 12184138—
반응물2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acidHCID 68703276—
반응물EDCl H2OHCID 87672115—
용매DimethylformamideHCID 6228—
생성물(r)-2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid (2-phenyl 1-pyrrolidin-1-ylmethylethyl)amideHCID 91139520—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07704996B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-ebbaec1b7fa74d20b57f0e984fa021c0
출처 메모uspto-grants-2010_04