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5-Nitroso-2,4,6-pyrimidinetriamine → 2,4,7-Triamino-6-(2-chlorophenyl)pteridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Nitroso-2,4,6-pyrimidinetriamine | HCID 70504 | — |
| 反応物 | (o-Chlorophenyl)acetonitrile | HCID 76112 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2,4,7-Triamino-6-(2-chlorophenyl)pteridine | HCID 15278935 | — |
反応手順
A stirred solution of 1.5 grams (0.010 mole) of 2,4,6-triamino-5-nitrosopyrimidine in 80 mL of N,N-dimethylformamide was heated to reflux, and 2.0 grams (0.01 3 mole) of 2-chlorophenylacetonitrile was added in one portion. Upon completion of addition, the reaction mixture was cooled, and 0.7 gram (0.013 mole) of sodium methoxide was added in one portion. The reaction mixture was again heated at reflux for 15 minutes. The reaction mixture was cooled in an ice-bath and then was filtered to collect a solid. The solid was slurried in diethyl ether and then was again collected by filtration, yielding, when dried, 2.5 grams of 2,4,7-triamino-6-(2-chlorophenyl)pteridine. The NMR spectrum was consistent with the proposed structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05521190 |
| 出典データセット | uspto-grants-1996_05 |
| ORD ID | ord-026491380cda4feb8509110ad50d91ee |
| 出典メモ | uspto-grants-1996_05 |