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Water → methyl 4-{[(3S)-1-(tert-butoxycarbonyl)piperidin-3-yl]amino}-6-iodoquinazoline-8-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | tert-butyl (3S)-3-aminopiperidine-1-carboxylate | HCID 1501975 | — |
| 反応物 | Methyl 4-chloro-6-iodoquinazoline-8-carboxylate | HCID 77231312 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | methyl 4-{[(3S)-1-(tert-butoxycarbonyl)piperidin-3-yl]amino}-6-iodoquinazoline-8-carboxylate | HCID 66763868 | 14.3% |
反応手順
Dissolved tert-butyl (35)-3-aminopiperidine-1-carboxylate (632.11 mg; 3.16 mmol; 1.10 eq.) in MeCN (18.00 ml) and TEA (1.00 ml). Added this mixture to methyl 4-chloro-6-iodoquinazoline-8-carboxylate (1000.00 mg; 2.87 mmol; 1.00 eq.). Stirred reaction at room temperature for 45 hours. LCMS indicated M+1=513 present. Diluted reaction with water and 1N NaOH. Filtered the resulting precipitate. Washed with water and dried to give a yellowish solid (210 mg). Carried material on without further purification. LCMS: M+1=513
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08637532B2 |
| 出典データセット | uspto-grants-2014_01 |
| ORD ID | ord-e86dd1e0306b49829c7fcbea9a8491cb |
| 出典メモ | uspto-grants-2014_01 |