HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-bromo-N,N-dimethylpyridin-2-amine → 4-((6-(dimethylamino)pyridin-2-yl)(hydroxy)(pyridin-2-yl)methyl)-6-(3,5-dimethylisoxazol-4-yl)-1H-benzo[d]imidazol-2(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-bromo-N,N-dimethylpyridin-2-amine | HCID 14006062 | — |
| Reactant | 6-(3,5-dimethylisoxazol-4-yl)-4-(hydroxy(6-methylpyridin-2-yl)(pyridin-2-yl)methyl)-1H-benzo[d]imidazol-2(3H)-one | HCID 86297160 | — |
| Product | 4-((6-(dimethylamino)pyridin-2-yl)(hydroxy)(pyridin-2-yl)methyl)-6-(3,5-dimethylisoxazol-4-yl)-1H-benzo[d]imidazol-2(3H)-one | HCID 117601948 | — |
Reaction Steps
A procedure similar to that used for 6-(3,5-dimethylisoxazol-4-yl)-4-(hydroxy(6-methylpyridin-2-yl)(pyridin-2-yl)methyl)-1H-benzo[d]imidazol-2(3H)-one, using 6-bromo-2-N,N-dimethylaminopyridine as the starting material was used to produce the intermediate (C32H36N6O5, 585.2 (M+1)), which was taken directly to the deprotection step to yield the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09255089B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-25971bb939fc490280371bcdeb585635 |
| Source note | uspto-grants-2016_02 |