関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | (1-methyl-1H-indazol-3-yl)methanol | HCID 7164546 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-(Bromomethyl)-1-methyl-1H-indazole | HCID 10775548 | 40.5% |
反応手順
To a stirring solution of 692 mg (2.64 mmol, 1.3 equiv) of triphenylphosphine in 10 mL of acetonitrile at 0° C. is added 125 μL (2.44 mmol, 1.2 equiv) of Br2. The resulting orange-yellow suspension is stirred 10 min at 0° C., then a solution of 330 mg (2.03 mmol) of (1-Methyl-1H-indazol-3-yl) methanol, prepared as in Intermediate 24, in 5 mL of acetonitrile is added over 2 min. The resulting solution is stirred 1.5 h at RT, and the solvent is removed in vacuo. Purification of the residue by silica gel flash column chromatography using hexane/EtOAc 5/1 as eluent afforded 185 mg of the title compound as a yellow solid: 1H NMR (CDCl3, 300 MHz) δ7.82 (d, 1H), 7.40 (m, 2H), 7.22 (m, 1H), 4.82 (s, 2H), 4.03 (s, 3H); Rf =0.87 in hexane/EtOAc 1/1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05859007 |
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| 出典データセット | uspto-grants-1999_01 |
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| ORD ID | ord-d14024e991324864af5109e900a8399e |
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| 出典メモ | uspto-grants-1999_01 |
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