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Nitric Acid → 2,4-Diamino-5-chloro-6-nitroquinazoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Nitric Acid | HCID 944 | — |
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | 2,4,6-Triamino-5-chloroquinazoline | HCID 152217 | — |
| 反応物 | 2,4-Quinazolinediamine, 5-chloro- | HCID 205130 | — |
| 反応物 | 2,4,6-Triaminoquinazoline | HCID 292661 | — |
| 生成物 | 2,4-Diamino-5-chloro-6-nitroquinazoline | HCID 12516826 | — |
反応手順
In a similar manner 2,4,6-triaminoquinazoline and 2,4,6-triamino-5-chloroquinazoline can be prepared. This is accomplished by the nitration of, for example, 2,4-diamino-5-chloroquinazoline (above) with 90% nitric acid and sulfuric acid, yielding the corresponding 2,4-diamino-5-chloro-6-nitroquinazoline. The 6-nitroquinazoline is in turn reduced by either hydrogenation in the presence of 10% palladium on carbon or by treatment with stannous chloride dihydrate, affording the corresponding 2,4,6-triaminoquinazoline. Steps A and B of Example 15 describe in detail these two steps in the reaction sequence.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05874579 |
| 出典データセット | uspto-grants-1999_02 |
| ORD ID | ord-7a1540adb5cf4a979b3e3c1263f63889 |
| 出典メモ | uspto-grants-1999_02 |