HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Morpholinophenyl)aminocarbonylbenzaldehyde → 4-(6-(4-Cyanobenzyloxy)-1H-benzo[d]imidazol-2-yl)-N-(4-morpholinophenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Morpholinophenyl)aminocarbonylbenzaldehyde | HCID 86673975 | — |
| Reactant | 1-(4-Cyanobenzyl)oxy-3,4-dinitrobenzene | HCID 86674011 | — |
| Product | 4-(6-(4-Cyanobenzyloxy)-1H-benzo[d]imidazol-2-yl)-N-(4-morpholinophenyl)benzamide | HCID 67686981 | — |
Reaction Steps
Compound 641 was prepared according to the procedure similar to that described in Scheme III from 1-(4-cyanobenzyloxy)-3,4-dinitrobenzene and 4-(4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C32H27N5O3: 530.21; found: 530.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09144557B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-20b1d94e018b4f4dbb6d469cfd9cbcf3 |
| Source note | uspto-grants-2015_09 |