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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10177생성일: 2026년 10월 23일

N,N,N',N'-Tetramethylethylenediamine → 4-Benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/10177

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물2-BromomethylnaphthaleneHCID 70320—
반응물Tert-butyl 4-benzylpiperazine-1-carboxylateHCID 584330—
반응물CID 53628100HCID 178418400—
용매Diethyl EtherHCID 3283—
생성물4-Benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl esterHCID 21041081—

반응 조건

온도-70 °C

반응 단계

To a solution of 4-benzyl-piperazine-1-carboxylic acid tert-butyl ester (2 g) in diethylether (35 mL) was added tetramethylethylenediamine (1.4 mL). The resulting mixture was cooled to −70° C. and sec-butyllithium (7 mL of a 1.3 M solution) was added dropwise, after complete addition the solution was slowly warmed to −10° C., at which temperature the mixture was stirred for one hour. Subsequently, the mixture was recooled to −70° C.; then a solution of 2-(bromomethyl)naphthalene (2 g) in diethylether was added dropwise and stirring continued at −70° C. was continued for one hour. The resulting mixture was stirred and allowed to come to room temperature overnight, then partitioned between saturated ammonium chloride (aq) and ethyl acetate. The organic layer was dried over magnesium sulphate, filtered, and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, CH2Cl2/MeOH 99/1) to afford 4-benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester as an oil. 0.8 g (27 %) Rf 0.47 (CH2Cl2/MeOH 99/1), MH+ 417.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094779B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-4894c875297347dab46acb76b5f533c2
출처 메모uspto-grants-2006_08