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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23209생성일: 2026년 10월 24일

Hydrochloric Acid → 1-Fmoc-4-Boc-Piperazine-2-acetic acid

https://huagongshe.com/ko/reaction/23209

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물9-Fluorenylmethyl chloroformateHCID 34367—
반응물Methyl 4-Boc-piperazine-2-acetateHCID 2756816—
용매TetrahydrofuranHCID 8028—
생성물1-Fmoc-4-Boc-Piperazine-2-acetic acidHCID 275679691.7%

반응 단계

A portion (5.2 g; 20 mmol) of the methyl 4-Boc-piperazine-2-acetate product from the previous step was combined with 60 mL of THF and 60 mL of 1 N NaOH (aqueous) and stirred at room temperature for 6 hours to saponify the methyl ester. The reaction was cooled to 0° C., adjusted to pH 9-10 with 10% HCl(aqueous), and 5.2 g (20 mmol) of FMOC-Cl was added. The reaction was stirred at room temperature for 6 hours, (adding 1 N NaOH (aqueous) to maintain pH 9-10) 1 hour, then acidified with 10% HCl to pH=1. The reaction was extracted twice, the combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo to give 8.56 g of the desired 4-Boc-1-Fmoc-piperazine-2-acetic acid (the compound of formula (XXIV)); 1H NMR (CDCl3) δ 1.4 (s,9), 2.5-3.0 (m,5) 3.9-4.2 (m,6), 4.5 (m,1), 7-25 (t,4), 7.32 (t,4), 7.48 (d,4), 7.75 (d, 4).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849739B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-1a9145d13d964fe58e1a408fd6fd08e6
출처 메모uspto-grants-2005_02