HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-amino-N,N-dimethylbenzylamine → N-(3-dimethylaminomethylphenyl)-2-[4-(6,7-dimethoxyquinazolin-4-yloxy)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-amino-N,N-dimethylbenzylamine | HCID 99294 | — |
| Reactant | 2-[4-(6,7-Dimethoxyquinazolin-4-yloxy)phenyl]acetic acid | HCID 66906632 | — |
| Product | N-(3-dimethylaminomethylphenyl)-2-[4-(6,7-dimethoxyquinazolin-4-yloxy)phenyl]acetamide | HCID 66906690 | 86% |
Reaction Steps
Using an analogous procedure to that described in Example 1, 2-[4-(6,7-dimethoxyquinazolin-4-yloxy)phenyl]acetic acid was reacted with 3-dimethylaminomethylaniline to give the title compound in 86% yield; 1H NMR: (DMSOd6) 2.14 (s, 3H), 3.35 (s, 2H), 3.68 (s, 2H), 3.97 (s, 3H), 3.99 (s, 3H), 6.96 (d, 1H), 7.24 (m, 1H), 7.26 (d, 2H), 7.39 (s, 1H), 7.44 (d, 2H), 7.53 (d, 1H), 7.55 (d, 1H), 7.58 (s, 1H), 8.53 (s, 1H), 10.19 (s, 1H); Mass Spectrum: M+H+ 473.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153643B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-00db25b057db4a5cae4238eb690dbfed |
| Source note | uspto-grants-2012_04 |