HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzyloxy-phenylboronic acid → 8-(4-Benzyloxy-phenyl)-6,7-dihydro-5H-1,4,8a-triaza-s-indacene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzyloxy-phenylboronic acid | HCID 2734314 | — |
| Reactant | 10-(4-benzyloxy-phenyl)-6,7,8,9-tetrahydro-5H-1,4,10a-triaza-cyclohepta[f]indene | HCID 58587717 | — |
| Reactant | 8-Chloro-6,7-dihydro-5H-1,4,8a-triaza-s-indacene | HCID 63820808 | — |
| Product | 8-(4-Benzyloxy-phenyl)-6,7-dihydro-5H-1,4,8a-triaza-s-indacene | HCID 69255282 | — |
Reaction Steps
Using the method described for the preparation of 10-(4-benzyloxy-phenyl)-6,7,8,9-tetrahydro-5H-1,4,10a-triaza-cyclohepta[f]indene, the reaction of 8-chloro-6,7-dihydro-5H-1,4,8a-triaza-s indacene and 4-benzyloxyphenyl boronic acid provided the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07319103B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-35fadcee45774c7bad1d92219ae0a454 |
| Source note | uspto-grants-2008_01 |