HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromopyridine-2-carbaldehyde → HCID 22143597, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromopyridine-2-carbaldehyde | HCID 2757009 | — |
| Reactant | 7-Chloro-2-(trimethylstannyl)thieno[3,2-b]pyridine | HCID 22143497 | — |
| Product | HCID 22143597 | HCID 22143597 | 27% |
Reaction Steps
This material was prepared by coupling 7-chloro-2-(trimethylstannyl)thieno[3,2-b]pyridine 39a (0.707 g, 2.17 mmole) with 6-bromopyridine-2-carbaldehyde (0.396 g, 2.17 mmole) using tereakis(triphenylphosphine)palladium(0) (100 mg) as catalyst in a manner as previously described for example 39b to give a white solid (0.161 g, 27%). 1H NMR (300 MHz, CDCl3) δ 10.15 (1H, s), 8.61 (1H, d, J=5.1 Hz), 7.93–8.09 (4H, m) 7.31 (1H, d, J=5.1 Hz); ESIMS (MH+): 275.00.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07045528B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-879c2e3565b047939eb9c11624a420ff |
| Source note | uspto-grants-2006_05 |