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HRID 243813作成日:2026年10月24日
Diisopropylethylamine → 1-(5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenyl)-3-((1S,2R)-1-hydroxy-2,3-dihydro-1H-indene-2-yl)urea
https://huagongshe.com/ja/reaction/243813
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | L-Tartaric acid | HCID 444305 | — |
| 反応物 | rac-(1R,2S)-2-amino-2,3-dihydro-1H-inden-1-ol | HCID 11008081 | — |
| 反応物 | 2,2,2-Trichloroethyl 5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenylcarbamate | HCID 68107458 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-(5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenyl)-3-((1S,2R)-1-hydroxy-2,3-dihydro-1H-indene-2-yl)urea | HCID 68107804 | 51% |
反応手順
To a solution of 2,2,2-trichloroethyl 5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenylcarbamate (0.086 g, 0.203 mmol) and (1S,2R)-2-amino-2,3-dihydro-1H-indene-1-ol.L-tartaric acid salt (0.067 g, 0.223 mmol) in acetonitrile (0.8 mL), N,N-diisopropylethylamine (0.058 mL, 0.333 mmol) was added, the mixture was stirred overnight at 110° C. The reaction mixture was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=10/90-60/40) to obtain 0.044 g of the captioned compound (51% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08653304B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-bcc932fdcde14f20ba571ba2466d1d37 |
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| 出典メモ | uspto-grants-2014_02 |
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