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2-Bromo-4-nitroquinoline → Tert-butyl methyl(4-(4-nitroquinolin-2-yl)phenyl)carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Bromo-4-nitroquinoline | HCID 581266 | — |
| 反応物 | tert-Butyl methyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate | HCID 4712653 | — |
| 生成物 | Tert-butyl methyl(4-(4-nitroquinolin-2-yl)phenyl)carbamate | HCID 58362579 | 68.5% |
反応手順
2-Bromo-4-nitroquinoline (50 mg, 0.2 mmol) and tert-butyl methyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate (66 mg, 0.2 mmol) were reacted using General Procedure (A) to afford tert-butyl methyl(4-(4-nitroquinolin-2-yl)phenyl)carbamate as a yellow oil (52 mg, 68%). 1H NMR (400 MHz, CDCl3): δ 8.43-8.40 (m, 2H), 8.28 (m, 1H), 8.19 (m, 2H), 7.87 (m, 1H), 7.73 (m, 1H), 7.46 (m, 2H), 3.35 (s, 3H), 1.59 (s, 3H), 1.50 (s, 9H); MS (ESI): 380 (M+H+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08491869B2 |
| 出典データセット | uspto-grants-2013_07 |
| ORD ID | ord-6487c09fe1e140b0ba0f5184a445e564 |
| 出典メモ | uspto-grants-2013_07 |