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1-Butanol, 4-bromo-, 1-acetate → 4-(2-Anilino-6-chloro-9H-purin-9-yl)butyl acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Butanol, 4-bromo-, 1-acetate | HCID 78491 | — |
| 反応物 | 9H-Purin-2-amine, 6-chloro-N-phenyl- | HCID 5271882 | — |
| 溶媒 | chloroform N,N-dimethylformamide | HCID 21754633 | — |
| 生成物 | 4-(2-Anilino-6-chloro-9H-purin-9-yl)butyl acetate | HCID 385891 | 45% |
反応手順
Reaction between 2-anilino-6-chloropurine and 4-acetoxybutyl bromide was performed as described in A.a., above, giving 2-anilino-6-chloro-9-(4-acetoxybutyl) purine in a 45% yield (from DMF/chloroform), mp 195°-197° C. 1H NMR δ9.98 (s, 2-NH), 8.32 (s, 8-H), 7.31 (m, C6H5), 4.20 (t, 1'-CH2), 4.02 (t, 4'-CH2), 1.95 (s, CH3), 1.92, 1.58 (m, 2'/3'CH2).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05646155 |
| 出典データセット | uspto-grants-1997_07 |
| ORD ID | ord-ac9a61d7a1d2420ebcca417076648ca9 |
| 出典メモ | uspto-grants-1997_07 |