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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645491생성일: 2026년 10월 25일

HOAt → 2-Cyano-4-(cyclohexylmethylamino)pyrimidine-5-carboxylic acid(2-morpholin-4-yl-1-phenylethyl)amide

https://huagongshe.com/reaction/645491

반응식

참여 물질

역할이름HCID투입량
반응물HOAtHCID 181649—
반응물2-(Morpholin-4-yl)-1-phenylethan-1-amineHCID 2814462—
반응물2-Cyano-4-(cyclohexylmethylamino)-pyrimidine-5-carboxylic acidHCID 68703380—
반응물EDCl H2OHCID 87672115—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-Cyano-4-(cyclohexylmethylamino)pyrimidine-5-carboxylic acid(2-morpholin-4-yl-1-phenylethyl)amideHCID 57580377—

반응 단계

To a solution of 2-cyano-4-(cyclohexylmethylamino)-pyrimidine-5-carboxylic acid (0.33 mmol, step 1.4) in DMF (2.0 mL) are added 2-morpholin-4-yl-1-phenylethylamine (69 mg, step 1.3), EDCl—H2O (0.50 mmol) and HOAt (0.50 mmol) at room temperature. After stirring at room temperature for 24 h, the reaction mixture is diluted with AcOEt. The mixture is washed with water, dried over Na2SO4, filtered, and concentrated in vacuo. The resulting residue is purified by RP-HPLC to give the title compound; 1H NMR (DMSO) δ 0.6-1.08 (m, 2H), 1.20-1.35 (m, 3H), 1.65-1.78 (m, 6H), 2.48-2.53 (m, 2H), 2.60-2.62 (m, 2H), 2.87-2.93 (m, 2H), 3.31-3.35 (m, 1H), 3.36-3.44 (M, 1H), 3.60-3.68 (m, 4H), 5.29-5.35 (m, 1H), 7.34-7.36 (m, 1H), 7.43-7.47 (m, 2H), 7.50-7.52 (m, 2H), 8.86 (s, 1H), 9.00-9.04 (m, 1H), 9.21 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07704996B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-aef23442ebd141288d5b04ce6fa32f44
출처 메모uspto-grants-2010_04