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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493395생성일: 2026년 10월 25일

N-(Diphenylmethylene)glycine tert-butyl ester → (2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoate

https://huagongshe.com/reaction/493395

반응식

참여 물질

역할이름HCID투입량
반응물N-(Diphenylmethylene)glycine tert-butyl esterHCID 688171—
반응물2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amineHCID 3513851—
반응물O-Allyl-N-(9-anthracenylmethyl)cinchonidinium bromideHCID 10886583—
반응물5-(Bromomethyl)-2-o-tolylpyridine hydrobromideHCID 67243566—
용매DichloromethaneHCID 6344—
생성물(2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoateHCID 86609629100%

반응 조건

온도-78 °C

반응 단계

To a stirred mixture of 800 mg (2.33 mmol) of 5-(bromomethyl)-2-o-tolylpyridine hydrobromide, 689 mg (2.33 mmol, 1.0 equivalent) of tert-butyl 2-(diphenylmethyleneamino)acetate and 141 mg (0.233 mmol, 0.1 equivalent) of O-allyl-N-(9-anthracenylmethyl) cinchonidinium bromide in 14 mL of dichloromethane at −78° C. under argon was added 1.687 mL (5.83 mmol, 2.5 eq) of 2-t-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine over 5 min. The reaction mixture was stirred at −78° C. for 10 h and then allowed to warm to room temperature in situ. The mixture was directly purified by silica gel chromatography using ethyl acetate/dichloro-methane (1:4) as eluant (5×10 cm column), to give tan oil, 1.10 g, 100% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534763B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-2297f5b0599e49ecbe788bdab41c8e13
출처 메모uspto-grants-2009_05