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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 396903생성일: 2026년 10월 24일

Boc-N-Me-Phe-OH → (2S)-6-[[(2S)-2-[tert-butoxycarbonyl(methyl)amino]-3-phenyl-propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acid

https://huagongshe.com/ko/reaction/396903

반응식

참여 물질

역할이름HCID투입량
반응물Boc-N-Me-Phe-OHHCID 7010602—
반응물Nalpha-isobutyl-Nalpha-(4-methylbenzenesulfonyl)-L-lysineHCID 23552860—
생성물(2S)-6-[[(2S)-2-[tert-butoxycarbonyl(methyl)amino]-3-phenyl-propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acidHCID 508602—

반응 단계

The title compound was prepared from Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-L-lysine (100 mg, 0.29 mmol, example 1, step E) as described in general procedure Bc using commercially available Nα-tert-butoxycarbonyl-Nα-methyl-L-phenylalanine (83 mg, 0.3 mmol). The final product was triturated with ether to yield 176 mg (90%) of the desired material.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608100B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-8c72e1815079491b8b6dbabae9163ec8
출처 메모uspto-grants-2003_08