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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 895461생성일: 2026년 10월 24일

N-(2-aminoethyl)acetamide → N-{2-[(6-amino-2-phenylpyrimidin-4-yl)amino]ethyl}acetamide

https://huagongshe.com/ko/reaction/895461

반응식

참여 물질

역할이름HCID투입량
반응물N-(2-aminoethyl)acetamideHCID 66082—
반응물6-Chloro-2-phenylpyrimidin-4-amineHCID 317747—
용매Ethyl AcetateHCID 8857—
생성물N-{2-[(6-amino-2-phenylpyrimidin-4-yl)amino]ethyl}acetamideHCID 22378791—

반응 단계

A solution of chloroarene 4 (20.57 g; 0.100 mol) in N-(2-aminoethyl)-acetamide (71.05 g; 0.696 mol) was heated from 60 to 120° C. over 20 min then kept at 120° C. for 4.0 h. After cooling to rt, the reaction was diluted with EtOAc (500 mL) then washed with water (1×150 mL). The aq phase was extracted with EtOAc (3×25 mL) and the combined organic portions were washed with water (2×25 mL) and saturated NaCl (2×50 mL). The solution was dried (MgSO4), filtered then concentrated in vacuo to 21.34 g of an off-white hard foam. The product was purified in two batches on silica gel (1.7 L total) using 15-8:1 DCM:MeOH yielding a hard white foam (15.36 g; 57%). LC (method B) tR=5.5 min; 1H NMR (200 MHz, CDCl3) δ 8.29 (m, 2H), 7.43 (m, 3H), 6.71 (brs, 1H), 5.41 (s, 1H), 5.12 (brt, J=5.4 Hz, 1H), 4.68 (brs, 2H), 3.53 (m, 1H), 3.45 (m, 1H), 1.83 (s, 3H); ESIMS 272.03 (100) [MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06916804B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-cac26463584b448bb719fa464f095cf7
출처 메모uspto-grants-2005_07