HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → 8-Ethynyl-1,6-naphthyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 8-Bromo-1,6-naphthyridine | HCID 817270 | — |
| Product | 8-Ethynyl-1,6-naphthyridine | HCID 74787874 | — |
Reaction Steps
The title compound can be synthesized from 8-ethynyl-1,6-naphthyridine and N-(3-(2-((dimethylamino)methyl)-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-iodo-4-methylbenzamide in a manner similar to that described for Example 1. 8-ethynyl-1,6-naphthyridine is prepared from 8-bromo-1,6-naphthyridine and ethynyltrimethylsilane according to the 2 steps procedure described in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461167B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-43136e85c1fc41a995e1fdc5fc275d50 |
| Source note | uspto-grants-2013_06 |