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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72132생성일: 2026년 10월 24일

Hydrochloric Acid → (R)-(2-adamantyl) 3-(isobutoxycarbonylamino)pyrrolidine-1-carboxylate

https://huagongshe.com/ko/reaction/72132

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물(3R)-(2-adamantyl) 3-(tert-butoxycarbonylamino)pyrrolidine-1-carboxylateHCID 52944645—
용매TetrahydrofuranHCID 8028—
생성물(R)-(2-adamantyl) 3-(isobutoxycarbonylamino)pyrrolidine-1-carboxylateHCID 5294217560.5%
생성물2-Adamantyl 3-(tert-butoxycarbonyl(methyl)amino)pyrrolidine-1-carboxylateHCID 58254875—

반응 조건

온도50 °C

반응 단계

2-adamantyl 3-(tert-butoxycarbonyl(methyl)amino)pyrrolidine-1-carboxylate was prepared as follows. A vial equipped with a flea stirbar was charged with (3R)-(2-adamantyl) 3-(tert-butoxycarbonylamino)pyrrolidine-1-carboxylate (105 mg, 0.29 mmol), methyl iodide (36 μL, 0.58 mmol) and dry THF (1 mL). 60% NaH in oil (14 mg, 0.58 mmol) was added and the mixture was stirred overnight under N2. The mixture was heated at 50° C. for 1 h, cooled and applied to a 10-mL ChemElut cartridge, prewetted with 5% aq HCl (6 mL), and eluted with ether (20 mL). The eluate was concentrated and the residue was purified by preparative HPLC to afford (R) 2-adamantyl 3-(tert-butoxycarbonyl(methyl)amino)pyrrolidine-1-carboxylate (32 mg, 29%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828985B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-bbaa93a5146b4d9d9957605f7bea428c
출처 메모uspto-grants-2014_09