HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → 4-Ethynylcinnoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 4-Bromocinnoline | HCID 57775218 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Ethynylcinnoline | HCID 57775151 | — |
Reaction Steps
The title compound can be synthesized from 4-ethynylcinnoline and N-(3-cyclopropyl-4-((4-methylpiperazin-1-yl)methyl)phenyl)-3-iodo-4-methylbenzamide in a manner similar to that described for Example 1 (nitro reduction performed in a manner similar to that described for Example 10; 0.25M in MeOH/10% AcOH). 4-ethynylcinnoline is prepared from 4-bromocinnoline 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-860136d3e644491f981dab7d679d053c |
| Source note | uspto-grants-2013_06 |