HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1-{4-[4-oxo-2-phenyl-7-(2H-pyrazol-3-yl)-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester → HCID 178452579, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1-{4-[4-oxo-2-phenyl-7-(2H-pyrazol-3-yl)-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester | HCID 67067641 | — |
| Reactant | {1-[4-(8-Bromo-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester | HCID 67067700 | — |
| Reactant | HCID 178431100 | HCID 178431100 | — |
| Product | HCID 178452579 | HCID 178452579 | 64% |
Reaction Steps
Following the procedure of (1-{4-[4-oxo-2-phenyl-7-(2H-pyrazol-3-yl)-4H-chromen-3-yl]-phenyl}-cyclobutyl)-carbamic acid tert-butyl ester, {1-[4-(8-bromo-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester was reacted with 3-(trifluoromethyl)-1H-pyrazole-4-boronic acid pinacol ester to give the title compound as a white solid (35 mg, 64%). LCMS (Method G): RT=4.15 min, [M+H]+=602.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546376B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-95f944078a5a4c6087d018db2aebd817 |
| Source note | uspto-grants-2013_10 |