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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1596464생성일: 2026년 10월 26일

1,1'-Carbonyldiimidazole → 3,4-Dimethoxyphenethyl 7-benzyl-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate

https://huagongshe.com/reaction/1596464

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물3,4-Dimethoxyphenethyl alcoholHCID 81911—
반응물3-Benzyl-3,7-diazabicyclo[3.3.1]nonaneHCID 13059482—
용매TetrahydrofuranHCID 8028—
생성물3,4-Dimethoxyphenethyl 7-benzyl-3,7-diazabicyclo[3.3.1]nonane-3-carboxylateHCID 2170193729%

반응 단계

3,4-Dimethoxyphenethyl alcohol (3.64 g; 20 mmol) was added to a stirred suspension of 1,1′-carbonyldiimidazole (3.24 g; 20 mmol) in THF (20 mL), and the mixture was refluxed for 12 h. A solution of 3-benzyl-3,7-diazabicyclo[3.3.1]nonane (4.33 g; 20 mmol; see Example E above) in THF (20 mL) was added and the reaction mixture was refluxed overnight. The solvent was removed and the residue dissolved in H2SO4 (2M; 25 mL) and extracted with diethyl ether. NaOH (3.5 mL; 5M) was added and the aqueous phase extracted with DCM. The organic layer was separated, dried and subjected to column chromatography (DCM:MeOH; gradient 0 to 30% MeOH) to give the sub-title compound in a 29% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06291475B1
출처 데이터셋uspto-grants-2001_09
ORD IDord-21b65b4160884ee58a89a1737c265300
출처 메모uspto-grants-2001_09