HuagongsheHuagongshe Chemistry Print Report · For research reference only
(E)-4-(5-Bromo-2-(2-(quinolin-2-yl)vinyl)imidazo[1,2-a]pyrazin-8-yl)morpholine → HCID 86345726, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (E)-4-(5-Bromo-2-(2-(quinolin-2-yl)vinyl)imidazo[1,2-a]pyrazin-8-yl)morpholine | HCID 117728505 | — |
| Reactant | HCID 131734681 | HCID 131734681 | — |
| Product | HCID 86345726 | HCID 86345726 | — |
Reaction Steps
Compound 2b was subjected to Suzuki coupling conditions using the methods described in Example 1, Step G, with compound 41b to obtain the title compound 20. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 8.35 (d, J=8.6 Hz, 1H), 8.18-8.20 (m, 2H), 8.15 (dd, J=8.6, 2.0 Hz, 1H), 7.96 (t, J=8.6 Hz, 2H), 7.90 (s, 1H), 7.86 (d, J=6.6 Hz, 1H), 7.72-7.80 (m, 2H), 7.64 (d, J=16.2 Hz, 1H), 7.56 (t, J=7.3 Hz, 1H), 7.49 (s, 1H), 4.31 (m, 4H), 3.80-3.86 (m, 4H), 3.58 (s, 3H), 3.28 (s, 3H). Mass Spectrum (LCMS, ESI pos.) Calcd. For C30H27N7O4S: 582.2 (M+H). Found 582.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249163B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-d3e71f0ff961457babff6a64d275f7a1 |
| Source note | uspto-grants-2016_02 |