HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methyl-4-anisidine → (4-Methoxy-phenyl)-methyl-quinazolin-4-yl-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methyl-4-anisidine | HCID 22250 | — |
| Reactant | 4-Chloroquinazoline | HCID 78864 | — |
| Product | (4-Methoxy-phenyl)-methyl-quinazolin-4-yl-amine | HCID 11254113 | — |
Reaction Steps
The title compound was prepared from 4-chloroquinazoline and 4-methoxy-N-methylaniline by a procedure similar to example 28 (79% yield). 1H NMR (CDCl3): 8.81 (s, 1H), 7.81 (d, J=8.1 Hz, 1H), 7.57 (ddd, J=8.1, 5.4 and 2.7 Hz, 1H), 7.09-7.14 (m, 2H), 7.03-7.06 (m, 2H), 6.9-6.93 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618975B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-5276d931959049589653d6bd271cf052 |
| Source note | uspto-grants-2009_11 |