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HRID 876013作成日:2026年10月25日
1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → (R)-t-butyl 2-((t-butyldimethylsilyloxy)methyl)-4-(6-chloropyridin-3-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/876013
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| 反応物 | 5-Bromo-2-chloropyridine | HCID 2734414 | — |
| 反応物 | Sodium t-butoxide | HCID 23676156 | — |
| 反応物 | (R)-t-Butyl 2-((t-butyldimethylsilyloxy)methyl)piperazine-1-carboxylate | HCID 58299667 | — |
| 触媒 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (R)-t-butyl 2-((t-butyldimethylsilyloxy)methyl)-4-(6-chloropyridin-3-yl)piperazine-1-carboxylate | HCID 86654440 | 48% |
反応手順
Compound 308 (361 mg, 1091 μmol), 5-bromo-2-chloropyridine (200 mg, 1039 μmol), Tris(dibenzylideneacetone)dipalladium (0) (71.4 mg, 77.9 μmol), 4,5-bis(diphenylphosphino)-9,9-dimethyl-9H-xanthene (90.2 mg, 156 μmol), and sodium t-butoxide (200 mg, 2079 μmol) were taken up in toluene (5 mL). The reaction was purged with argon and heated at 80° C. for 5 hours. The resulting solution was added to aqueous K2CO3 (10%, 30 mL) and extracted with dichloromethane+10% methanol (3×30 mL). The combined organics were dried (MgSO4) and evaporated to give an orange tar. Silica gel chromatography (gradient elution hexanes/0-20% ethyl acetate) afforded compound 309 as a pale yellow oil (219 mg, 48%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08980903B2 |
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| 出典データセット | uspto-grants-2015_03 |
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| ORD ID | ord-fde823539bd143b3aaa12a80f2da9c85 |
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| 出典メモ | uspto-grants-2015_03 |
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