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Ammonium Hydroxide → 9-Butyl-8-(2,5-Dimethoxy-Benzyl)-9h-Purin-6-Ylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 反応物 | 6-chloro-8-(2,5-dimethoxybenzyl)-N9-butyl purine | HCID 85827657 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 9-Butyl-8-(2,5-Dimethoxy-Benzyl)-9h-Purin-6-Ylamine | HCID 448969 | — |
反応手順
To a solution of 6-chloro-8-(2,5-dimethoxybenzyl)-N9-butyl purine (1 mmol) in dioxane was added 28% NH4OH (50 mmol) and the mixture was then heated at 100 C in a seal tube for 48 h. Solvent was removed by azeotrope distillation with toluene. Purification on a silica gel column (see above) gave pure 8-(2,5-dimethoxybenzyl)-9-butyl adenine, 1.1. Rf=0.35 in 5% MeOH in EtOHAc. 1H NMR (DMSO-d6) δ 8.08 (s, 1H), 7.04 (br s, 2H), 6.94 (d, 1H), 6.80 (dd, 1H), 6.66 (d, 1H), 4.14 (s, 2H), 4.04 (t, 2H), 3.72 (s, 3H), 3.63 (s, 3H), 1.52 (m, 2H), 1.22 (m, 2H), 0.82 (t, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07241890B2 |
| 出典データセット | uspto-grants-2007_07 |
| ORD ID | ord-51eca18288364916976b90311ead8a22 |
| 出典メモ | uspto-grants-2007_07 |