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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3292생성일: 2026년 10월 23일

Hydrochloric Acid → 7a-(5-Pyrimidinyl)-hexahydro-1h-pyrrolizine

https://huagongshe.com/ko/reaction/3292

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물5-BromopyrimidineHCID 78344—
반응물Pyrrolizinium, 1,2,3,5,6,7-hexahydro-, perchlorateHCID 10878400—
반응물HCID 178418306HCID 178418306—
용매Diethyl EtherHCID 3283—
용매PentaneHCID 8003—
용매Ether tetrahydrofuranHCID 21868444—
생성물7a-(5-Pyrimidinyl)-hexahydro-1h-pyrrolizineHCID 1893476818%

반응 조건

온도0 °C

반응 단계

A solution of 1.7M tBuLi (1.6 mL, 2.6 mmol) in pentane was added to 5-bromopyrimidine (190 mg, 1.2 mmol) in Et2O:THF (1:1, 12 mL) at -100° C. After stirring for 10 minutes, 1,2,3,5,6,7-hexahydropyrrolizinium perchlorate (500 mg, 2.4 mmol) was added to the reaction slurry, and stirring was continued for 30 minutes. The reaction mixture was then allowed to warm to 0° C. and stir for 1 hour. A solution of 2N HCl was added, and the reaction mixture was poured over Et2O and the phases separated. The aqueous phase was basified with 15% NaOH solution and extracted with CH2Cl2 (2×). The CH2Cl2 phases were combined, dried (MgSO4), concentrated, and the residue was chromatographed (silica gel; CHCl3 /MeOH, 98:2) to afford a clear oil (40 mg, 18%). MS (CI/NH3) m/e: 190 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ1.60-1.73 (m, 2H), 1.82-2.11 (m, 6H), 2.66-2.75 (m, 2H), 3.15-3.21 (m, 2H), 8.85 (s, 2H), 9.05 (s,1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733912
출처 데이터셋uspto-grants-1998_03
ORD IDord-00d6327228e6450289cc61943cc4bea5
출처 메모uspto-grants-1998_03