HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → {4-[1-(4-Chloro-phenyl)-1-methyl-ethyl]-5-methyl-pyrimidin-2-yl}-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(4-Chloro-phenyl)-1-dimethylamino-4-methyl-pent-1-en-3-one | HCID 68630377 | — |
| Reactant | HCID 178493228 | HCID 178493228 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | {4-[1-(4-Chloro-phenyl)-1-methyl-ethyl]-5-methyl-pyrimidin-2-yl}-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine | HCID 44192989 | — |
Reaction Steps
The title compound was prepared in analogous manner as described in example 4c) from N-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]guanidine dinitrate, 4-(4-chloro-phenyl)-1-dimethylamino-4-methyl-pent-1-en-3-one, and triethylamine using 1-methyl-2-pyrrolidone as solvent. The reaction was performed in a microwave at 200° C. for 2.5 h. The title compound was isolated as a yellow solid in 52% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08962834B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-37ea9e8537d14a6688d13c365d3894bd |
| Source note | uspto-grants-2015_02 |