HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → HCID 86297146, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 90411755 | HCID 90411755 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86297146 | HCID 86297146 | — |
Reaction Steps
Compound 31 was synthesized using N-(3-(6-bromoimidazo[1,2-a]pyrimidin-2-yl)-4-chlorophenyl)-5-methylfuran-2-carboxamide (I-14) as the bromide and phenylboronic acid using a suzuki coupling protocol described in the synthesis of I-11. The residue was redissolved in methanol and precipitation yielded the compound 1H NMR (400 MHz, DMSO-D6) δ 10.33 (s, 1H), 9.38 (d, J=2.1, 1H), 8.99 (d, J=2.0, 1H), 8.71 (d, J=2.5, 1H), 8.62 (s, 1H), 7.95 (dd, J=2.4, 8.7, 1H), 7.80 (d, J=7.8, 2H), 7.52 (dt, J=7.8, 14.7, 5H), 7.34 (d, J=3.3, 1H), 6.35 (d, J=3.3, 1H), 2.40 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296754B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-b6b292d9f42d40068bed8f090948b583 |
| Source note | uspto-grants-2016_03 |