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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 505425생성일: 2026년 10월 26일

Diisopropylethylamine → N-(2-Amino-5-iodo-pyridin-3-yl)-3-[4-methyl-6-(trityl-amino)-pyridin-2-yl]-propionamide

https://huagongshe.com/reaction/505425

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5-Iodopyridine-2,3-diamineHCID 21882766—
반응물3-[4-Methyl-6-(trityl-amino)-pyridin-2-yl]propionic acidHCID 68461590—
용매PyridineHCID 1049—
생성물N-(2-Amino-5-iodo-pyridin-3-yl)-3-[4-methyl-6-(trityl-amino)-pyridin-2-yl]-propionamideHCID 6846109754.9%

반응 조건

온도50 °C

반응 단계

1.30 g of 3-[4-methyl-6-(trityl-amino)-pyridin-2-yl]-propionic acid acid and 724 mg of 2,3-diamino-5-iodo-pyridine are dissolved in 37 ml of pyridine and sequentially treated with 1.06 g of O-[(ethoxycarbonyl)canomethylene-amino]—N,N,N′,N′-tetramethyl-uronium tetrafluoro-borate and 579 μl of diisopropylethyl amine. The reaction mixture is warmed to 50° C. for 24 h. Thereafter the solvents are evaporated in vacuo. The remaining residue is coevaporated twice with toluene yielding 3.55 g of crude product. Purification by chromatography on LiChroprep® NH2 (25-40 μm, Merck, Darmstadt) (75 g, eluent: toluene/ethyl acetate 1:1) affords 1.08 g of the title compound as an amorphous solid. ESI-MS: 640.0 (MH+). TLC: Rf=0.16 (toluene/ethyl acetate 1:1, LiChroprep® NH2 HPTLC).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07781453B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-3a7d2db97ccf4dcea8e6c9280c3f517c
출처 메모uspto-grants-2010_08