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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1488254생성일: 2026년 10월 27일

Potassium Carbonate → 2,2'-[(2-{[3-(Benzyloxy)-3-oxopropyl]amino}-2-oxoethyl)imino]diacetic acid

https://huagongshe.com/reaction/1488254

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,6-dioxo-N-(carboxymethyl)morpholineHCID 169531—
반응물Benzyl 3-aminopropanoate hydrochlorideHCID 19434764—
용매DimethylformamideHCID 6228—
생성물2,2'-[(2-{[3-(Benzyloxy)-3-oxopropyl]amino}-2-oxoethyl)imino]diacetic acidHCID 117996360—

반응 단계

To an ice bath cooled solution of benzyl 3-aminopropanoate hydrochloride (4.49 g, 20.8 mmol) in DMF (30 mL) was added K2CO3 (3.02 g, 21.84 mmol) and the resulting mixture was stirred at o° C. for 2 hr. The mixture was then filtered and the filtrate was added to an ice bath cooled solution of 2-(2,6-dioxomorpholino)acetic acid (4.47 g, 25.8 mmol) in DMF (30 mL). The resulting mixture was stirred at 0° C. for 30 min, then at rt for 2 hr. The reaction was quenched by the addition of water (30 mL) and the resulting mixture was concentrated. The residue was stirred with water (40 mL), and the resulting precipitate was collected through filtration and dried to give the title compound. 1H NMR (DMSO-d6) δ 2.53 (t, J=6.8, 2H), 3.27 (s, 2H), 3.36 (q, J=6.2, 2H), 3.42 (m, m 2H), 3.49 (s, 2H), 5.09 (s, 2H), 7.28 (m, 4H), 8.16 (m, 1H), 12.45 (br s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09427475B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-017ba17c0fc54d9ab0d8a33f5cfce7fa
출처 메모uspto-grants-2016_08