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HRID 2220256作成日:2026年10月27日
N-(Diphenylmethylene)glycine tert-butyl ester → (2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoate
https://huagongshe.com/reaction/2220256
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | N-(Diphenylmethylene)glycine tert-butyl ester | HCID 688171 | — |
| 反応物 | 2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amine | HCID 3513851 | — |
| 反応物 | O-Allyl-N-(9-anthracenylmethyl)cinchonidinium bromide | HCID 10886583 | — |
| 反応物 | 5-(Bromomethyl)-2-o-tolylpyridine hydrobromide | HCID 67243566 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoate | HCID 86609629 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07417028B2 |
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| 出典データセット | uspto-grants-2008_08 |
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| ORD ID | ord-2f2c7abd700541a3be7adfe2c51eb938 |
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| 出典メモ | uspto-grants-2008_08 |
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