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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 396914생성일: 2026년 10월 24일

3-Aminopyridine → (2S)-2-[isobutyl(p-tolylsulfonyl)amino]-6-[[2-(3-pyridylamino)acetyl]amino]hexanoic acid

https://huagongshe.com/ko/reaction/396914

반응식

참여 물질

역할이름HCID투입량
반응물3-AminopyridineHCID 10009—
반응물DiisopropylethylamineHCID 81531—
반응물Nalpha-isobutyl-Nalpha-(4-methylbenzenesulfonyl)-Nepsilon-iodoacetyl-L-lysineHCID 86589941—
생성물(2S)-2-[isobutyl(p-tolylsulfonyl)amino]-6-[[2-(3-pyridylamino)acetyl]amino]hexanoic acidHCID 508627—

반응 단계

The title compound was prepared from Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-Nε-iodoacetyl-L-lysine (200 mg, 0.38 mmol, example 105, step B) by following the indications of general procedure H using DIEA (0.19 mL, 1.09 mmol) and 3-aminopyridine (175 mg, 1.36 mmol). The crude material was purified by preparative HPLC. The product was isolated as a solid (42 mg, 22% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608100B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-8d41696b5a64439b8cf914556d49ae93
출처 메모uspto-grants-2003_08