HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenylboronic acid → HCID 68439640, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenylboronic acid | HCID 2734615 | — |
| Reactant | HCID 86606279 | HCID 86606279 | — |
| Product | HCID 68439640 | HCID 68439640 | 57% |
Reaction Steps
The title compound was then prepared according to the Suzuki coupling procedure of Example 35, step (b) using 4-aminophenylboronic acid (219 mg, 1.00 mmol) and cis/trans-2,6-dimethyl-4-trifluoromethanesulfonyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (as prepared above, 321 mg, 1.00 mmol). Silica gel chromatography (10-20% EtOAc/hexanes) afforded 4-(4-amino-phenyl)-2,6-dimethyl-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (172 mg, 57%): Mass spectrum (ESI, m/z): Calcd. for C18H26N2O2, 303.2 (M+H) found 303.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645755B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-e1152a0429e3476d87dc43c79017b735 |
| Source note | uspto-grants-2010_01 |