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HRID 493395作成日:2026年10月26日

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

https://huagongshe.com/reaction/493395

反応式

関与物質

役割名称HCID仕込み量
反応物N-(Diphenylmethylene)glycine tert-butyl esterHCID 688171—
反応物2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amineHCID 3513851—
反応物O-Allyl-N-(9-anthracenylmethyl)cinchonidinium bromideHCID 10886583—
反応物5-(Bromomethyl)-2-o-tolylpyridine hydrobromideHCID 67243566—
溶媒DichloromethaneHCID 6344—
生成物(2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoateHCID 86609629100%

反応条件

温度-78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534763B2
出典データセットuspto-grants-2009_05
ORD IDord-2297f5b0599e49ecbe788bdab41c8e13
出典メモuspto-grants-2009_05