HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → HCID 86297147, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | 4-(Methoxycarbonylamino)phenylboronic acid | HCID 2773494 | — |
| Reactant | HCID 90444848 | HCID 90444848 | — |
| Product | HCID 86297147 | HCID 86297147 | — |
Reaction Steps
Compound 32 was synthesized using 2-methoxyethyl (3-(6-bromoimidazo[1,2-a]pyrimidin-2-yl)-4-chlorophenyl)carbamate (I-12) as the bromide and (4-((methoxycarbonyl)amino)phenyl)boronic acid using a suzuki coupling procedure described in I-13. Purification of the compound was done via mass-triggered reverse phase column chromatography preparative system (15% to 65% (B)). m/z (ESI) for 32: 496 (M+H+), 1H NMR (600 MHz, DMSO-D6) δ 10.01 (s, 1H), 9.86 (s, 1H), 9.30 (s, 1H), 8.95 (s, 1H), 8.55 (s, 1H), 8.47 (s, 1H), 7.72 (d, J=6.0, 2H), 7.62 (d, J=6.6, 2H), 7.50 (dt, J=5.7, 8.5, 2H), 4.24 (s, 2H), 3.70 (s, 3H), 3.59 (s, 2H), 3.30 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296754B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-70b874e276074920ac8078101685a55a |
| Source note | uspto-grants-2016_03 |