HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10556Generated: October 29, 2026
Tris(1,1-dimethylethyl)phosphine → HCID 178419024, compound
https://huagongshe.com/reaction/10556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | 5-Bromo-4-methylisoquinoline | HCID 21979882 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 178418966 | HCID 178418966 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178419024 | HCID 178419024 | — |
Reaction Steps
According to the method of Example 15, Step A, the title compound was synthesized from Intermediate 93. That is, under nitrogen atmosphere, a suspension of Intermediate 93 (602 mg), tris(dibenzylideneacetone)dipalladium(0) (124 mg), tri(tert-butyl)phosphine (0.5 ml, Kanto Chemicals), cis-N-(tert-butoxycarbonyl)-1,4-cyclohexanediamine (697 mg) and sodium tert-butoxide (390 mg) in toluene was stirred with heating at 120° C. for 16.5 hours. The reaction mixture was cooled to room temperature and added with ethyl acetate (10 ml), and the insoluble matters were removed by filtration through Celite. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to obtain the title compound (45 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07094789B2 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-2ef5bc5c67c04ed392a15b43bd1a3710 |
|---|
| Source note | uspto-grants-2006_08 |
|---|