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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1267503생성일: 2026년 10월 26일

Potassium Carbonate → N,N-Diethyl-4-[(8-azabicyclo[3.2.1]oct-3-ylidene)phenylmethyl]benzamide Hydrochloride

https://huagongshe.com/reaction/1267503

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,2,2-Trichloroethyl chloroformateHCID 87063—
반응물N,N-diethyl-4-[(8-methyl-8-azabicyclo[3.2.1]oct-3-ylidene)phenylmethyl]benzamideHCID 9952263—
촉매ZincHCID 23994—
용매BenzeneHCID 241—
생성물N,N-Diethyl-4-[(8-azabicyclo[3.2.1]oct-3-ylidene)phenylmethyl]benzamide HydrochlorideHCID 18545680—

반응 단계

A 100 mL benzene suspension of 3.1 g (5.6 mmol) N,N-diethyl-4-[(8-methyl-8-azabicyclo[3.2.1]oct-3-ylidene)phenylmethyl]benzamide, 3.45 g (25 mmol) K2CO3, and 1.5 mL (10 mmol) 2,2,2-trichloroethyl chloroformate was allowed to reflux for 2 h. The reaction was cooled, filtered, and the solvent evaporated. The residual oil was dissolved in MeOH then stirred at reflux with 2.6 g (40 mmol) zinc powder for 1 h. After cooling, the reaction was filtered through celite and partitioned between 3N NaOH and CH2Cl2. The organic layer was washed with brine, dried over K2CO3, filtered, and concentrated (2.1 g, 5.6 mmol). The resulting clear oil was dissolved in Et2O, filtered, and the product precipitated after the addition of ethereal HCl; mp 128-132° C. MS m/z (MH+) 375. 1H NMR 300 MHz (DMSO-d6) δ 7.15-7.4 (m, 9H), 3.9-4.0 (m, 2H), 3.15-3.3 (m, 2H), 2.55-2.65 (m, 2H), 2.25-2.35 (m, 4H), 1.9-2.0 (m, 2H), 1.75-1.85 (m, 2H), 1.0-1.2 (m, 6H). Anal calc C25H30N2O.HCl (3% H2O): C, 70.89; H, 7.71; N, 6.61. Found: C, 70.52; H, 7.41; N, 6.24.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06552036B2
출처 데이터셋uspto-grants-2003_04
ORD IDord-cff11921d3cc40f99a6e17f26982e00d
출처 메모uspto-grants-2003_04