HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenylcyclohexanone → HCID 483228, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenylcyclohexanone | HCID 78605 | — |
| Reactant | HCID 178418324 | HCID 178418324 | — |
| Product | HCID 483228 | HCID 483228 | — |
Reaction Steps
This compound was prepared in a manner analogous to that of Example 1, using 4.2 grams (0.05 mole) of cyanoguanidine and 13.1 grams (0.08 mole) of 4-phenylcyclohexanone. The crude product was recrystallized from ethanol, yielding 2,4-diamino-6-phenyl-5,6,7,8-tetrahydroquinazoline, mp 223°-226° C. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05712281 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-5e09201d69a8448fbe8aebde8306b0c8 |
| Source note | uspto-grants-1998_01 |