HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromoisoquinoline → HCID 11391278, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromoisoquinoline | HCID 73743 | — |
| Reactant | 1-Ethynyl-4-methoxybenzene | HCID 251020 | — |
| Product | HCID 11391278 | HCID 11391278 | 59% |
Reaction Steps
According to Scheme 29 Step 1: The title compound was prepared from 4-bromoisoquinoline (1 eq, 5.30 mmol, 1.10 g) and 1-ethynyl-4-methoxybenzene (1 eq, 5.30 mmol, 0.70 g) according to the procedure described for Example 13 Step 1. Reaction conditions: 70° C. for 4 hours. The crude product was purified by silica gel chromatography (AIT Flashsmart prepacked column SiO2, cyclohexane/AcOEt 90/10 to 80/20) to afford 4-(2-(4-methoxyphenyl)ethynyl)isoquinoline (3.11 mmol, 0.81 g, 59%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399493B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-6f966d89fd5f422d9ac28d1bf1a1fd55 |
| Source note | uspto-grants-2013_03 |