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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397801생성일: 2026년 10월 23일

4-Aminopyridine → (2S)-2-[isobutyl(p-tolylsulfonyl)amino]-6-[[2-(4-pyridylamino)acetyl]amino]hexanoic acid

https://huagongshe.com/ko/reaction/397801

반응식

참여 물질

역할이름HCID투입량
반응물4-AminopyridineHCID 1727—
반응물DiisopropylethylamineHCID 81531—
반응물Nalpha-isobutyl-Nalpha-(4-methylbenzenesulfonyl)-Nepsilon-iodoacetyl-L-lysineHCID 86589941—
생성물(2S)-2-[isobutyl(p-tolylsulfonyl)amino]-6-[[2-(4-pyridylamino)acetyl]amino]hexanoic acidHCID 508634—

반응 단계

The title compound was prepared from Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-Nε-iodoacetyl-L-lysine (150 mg, 0.29 mmol, example 105, step B) by following the indications of general procedure H using DIEA (0.10 mL, 0.57 mmol) and 4-aminopyridine (76 mg, 0.59 mmol). The crude material was purified by preparative HPLC. The product was isolated as a solid (39 mg, 28% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610689B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-c775585ddd084d728a490f8d36335ebe
출처 메모uspto-grants-2003_08