HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-6-methylbenzonitrile → Quinazoline, 2,4-diamino-5-methyl-(7CI,8CI)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-6-methylbenzonitrile | HCID 279973 | — |
| Reactant | Chloroformamidinium chloride | HCID 3084509 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | Quinazoline, 2,4-diamino-5-methyl-(7CI,8CI) | HCID 198062 | 86.9% |
Reaction Steps
This compound was prepared in a manner analogous to that of Step E of Example 1, using 10.0 grams (0.076 mole) of 2-amino-6-methylbenzonitrile (prepared as in Example 1, Step B), and 10.0 grams (0.087 mole) of chloroformamidine hydrochloride in 40 mL of 2-methoxyethyl ether, yielding 11.5 grams of 2,4-diamino-5-methylquinazoline. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05534518 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-2b2a890cd01b4ee9ac25ab096046fc03 |
| Source note | uspto-grants-1996_07 |