HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-5-methyl-o-anisidine → (S)-2-Amino-6-(5-(4-chloro-2-methoxy-5-methylphenylamino)-2-fluorophenyl)-3,5,5,6-tetramethyl-5,6-dihydropyrimidin-4(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-5-methyl-o-anisidine | HCID 80782 | — |
| Reactant | (S)-2-{[bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-6-(5-bromo-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-one | HCID 57497159 | — |
| Product | (S)-2-Amino-6-(5-(4-chloro-2-methoxy-5-methylphenylamino)-2-fluorophenyl)-3,5,5,6-tetramethyl-5,6-dihydropyrimidin-4(3H)-one | HCID 57497042 | — |
Reaction Steps
The coupling (S)-2-{[bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-6-(5-bromo-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-one (intermediate K) and 4-chloro-2-methoxy-5-methyl-phenylamine according to procedure B followed by deprotection yielded the title compound as an off-white solid. MS (ESI): m/z=433.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815881B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-5beb18ad8af245628a314fefd2d66eb6 |
| Source note | uspto-grants-2014_08 |