HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 2,4-Diamino-5-chloro-6-nitroquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,4,6-Triamino-5-chloroquinazoline | HCID 152217 | — |
| Reactant | 2,4-Quinazolinediamine, 5-chloro- | HCID 205130 | — |
| Reactant | 2,4,6-Triaminoquinazoline | HCID 292661 | — |
| Product | 2,4-Diamino-5-chloro-6-nitroquinazoline | HCID 12516826 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05534518 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-ff8313b0045648b38ce8f4c5fa50953e |
| Source note | uspto-grants-1996_07 |