HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → HCID 86281290, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | 4-(Methoxycarbonylamino)phenylboronic acid | HCID 2773494 | — |
| Reactant | HCID 90412061 | HCID 90412061 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86281290 | HCID 86281290 | — |
Reaction Steps
Compound 24 was synthesized using N-(3-(6-bromoimidazo[1,2-a]pyrimidin-2-yl)-4-chlorophenyl)pyrrolidine-1-carboxamide (I-15) as the bromide and (4-((methoxycarbonyl)amino)phenyl)boronic acid using a suzuki coupling protocol as described in the synthesis of I-11. The residue was redissolved in methanol and precipitation yielded the compound. m/z (ESI) of 24: 491.2 (M+H+), 1H NMR (600 MHz, DMSO-D6) δ 9.86 (s, 1H), 9.30 (d, J=2.6, 1H), 8.94 (d, J=2.6, 1H), 8.55 (s, 1H), 8.47 (d, J=2.8, 2H), 7.73 (m, 3H), 7.62 (d, J=8.5, 2H), 7.41 (d, J=8.8, 1H), 3.70 (s, 3H), 3.40 (t, J=6.5, 4H), 1.86 (t, J=6.4, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296754B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-e2b78c93d71d49309b6bd76f6ef91a7f |
| Source note | uspto-grants-2016_03 |