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1-methyl-2-(tributylstannyl)-1H-pyrrole → 1-[3-(1-methyl-1H-pyrrol-2-yl)phenyl]-N-(Pyridin-3-ylmethyl)-1H-benzimidazole-5-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-methyl-2-(tributylstannyl)-1H-pyrrole | HCID 2769397 | — |
| 反応物 | 1-(3-bromophenyl)-N-pyridin-3-ylmethyl-1H-benzimidazole-5-carboxamide | HCID 57639717 | — |
| 触媒 | HCID 178418476 | HCID 178418476 | — |
| 生成物 | 1-[3-(1-methyl-1H-pyrrol-2-yl)phenyl]-N-(Pyridin-3-ylmethyl)-1H-benzimidazole-5-carboxamide | HCID 11553258 | — |
反応手順
A mixture of 1-(3-bromophenyl)-N-pyridin-3-ylmethyl-1H-benzimidazole-5-carboxamide (85 mg, 0.209 mmol), Pd(PPh3)2Cl2 (28 mg, 0.040 mmol) and Ag2O (45 mg, 0.196 mmol) was added in one portion to a flask charged with 1-methyl-2-tributylstannanyl-1H-pyrrole (0.391 g, 1.06 mmol). The flask was evacuated and backfilled with N2 (2×) then charged with anhydrous DMF (3.0 mL). After stirring at rt for 5 min the reaction mixture was heated to 90° C. under N2 for 2 d. Later, the reaction was cooled to rt and treated with 1 M aq KF (3 mL) and stirred overnight at rt. Then filtered through Celite (using MeOH to rinse the Celite) and purified by MDPS to provide the product as a white solid. MS (ES+): m/z 408.46 (100) [MH+].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07419995B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-6be9645c11bd4801a0a39a2ece2197db |
| 出典メモ | uspto-grants-2008_09 |