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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 869생성일: 2026년 10월 23일

Potassium bisulfate → benzyl N-[3-(2-aminoethyl)pyrrolidine-1-carboximidoyl]carbamate

https://huagongshe.com/ko/reaction/869

반응식

참여 물질

역할이름HCID투입량
반응물Potassium bisulfateHCID 516920—
반응물tert-butyl N-[2-(pyrrolidin-3-yl)ethyl]carbamateHCID 21955469—
반응물Benzyl [amino(methylsulfanyl)methylene]carbamateHCID 140362141—
용매TolueneHCID 1140—
생성물benzyl N-[3-(2-aminoethyl)pyrrolidine-1-carboximidoyl]carbamateHCID 14037908367.5%

반응 단계

2.18 g (0.0102 mole) (3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine and 2.81 g (0.0125 mole) N-benzyloxycarbonyl-S-methylisothiourea was dissolved in 30 ml toluene and heated to 60°-70° C. for eight hours followed by stirring at room temperature for one day. 0.3M KHSO4 -solution was added and the water layer was washed with a mixture of the toluene and ethyl acetate and left for 2 days under which time the Boc group was removed. The acidic water phase was made alkaline and extracted four times with CH2 Cl2. The combined organic layer was dried (Na2SO4), filtered and evaporated to yield 2.0 g (51%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723444
출처 데이터셋uspto-grants-1998_03
ORD IDord-d42f48a7d3fc473aba6c5139093935b5
출처 메모uspto-grants-1998_03