化工社化工社 化学情報印刷レポート · 研究参考用
Acetonitrile → n-[4-(2,4-Dioxo(1,3-dihydroquinazolin-3-yl))phenyl]{[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amino}carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 反応物 | 3-(4-Aminophenyl)-1,3-dihydroquinazoline-2,4-dione trifluoroacetate | HCID 22064391 | — |
| 反応物 | (Tert-butyl)[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amine | HCID 22064462 | — |
| 溶媒 | Trifluoroacetic acid | HCID 6422 | — |
| 生成物 | n-[4-(2,4-Dioxo(1,3-dihydroquinazolin-3-yl))phenyl]{[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amino}carboxamide | HCID 22064426 | 34% |
反応手順
A 19 mg-sample (0.07 mmol) of (tert-butyl)[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amine was dissolved in neat TFA and stirred for 1 h, concentrated in vacuo and used directly in the next transformation. This sample was dissolved in 150 uL of DCM and 21 mg (0.084 mmol) of DSC was added followed by 21 μL (0.14 mmol) of DBU. This solution was stirred for 18 h, 26 mg (0.07) of 3-(4-aminophenyl)-1,3-dihydroquinazoline-2,4-dione trifluoroacetate salt was added plus 150 μL of dry acetonitrile and refluxed for 2 h. This material was then purified on RP-HPLC to afford 11 mg (34%) of the desired product. BS-MS: M+H+=495 (Cl).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524721B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-c402dd8d3437460b920d5e0d79eff05a |
| 出典メモ | uspto-grants-2013_09 |