HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenamine, N,4-dimethyl- → 4-Quinazolinamine, 2-chloro-N-methyl-N-(4-methylphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenamine, N,4-dimethyl- | HCID 12165 | — |
| Reactant | 2,4-Dichloroquinazoline | HCID 252886 | — |
| Product | 4-Quinazolinamine, 2-chloro-N-methyl-N-(4-methylphenyl)- | HCID 11266078 | — |
Reaction Steps
The title compound was prepared from 2,4-dichloroquinazoline (250 mg, 1.25 mmol) and 4-methyl-N-methylaniline (196 mg, 1.43 mmol) by a procedure similar to example 1b and was isolated as white powder (210 mg, 84%). 1H NMR (CDCl3): 8.69 (d, J=8.4 Hz, 1H), 7.75 (dd, J=8.1 and 7.5 Hz, 1H), 7.39 (d, J=7.8 Hz, 2H), 7.25 (d, J=7.8 Hz, 2H), 7.13 (d, J=8.2 Hz, 1H), 6.74 (d, J=8.7 Hz, 1H), 3.81 (s, 3H), 2.49 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258145B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-526a4e6586264fe6a16c99b7268754f3 |
| Source note | uspto-grants-2012_09 |