HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 57443610, compound → HCID 86610107, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 57443610 | HCID 57443610 | — |
| Reactant | 3-Chloro-5-(2-chloro-5-ethynylphenoxy)benzonitrile | HCID 57443613 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178479804 | HCID 178479804 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86610107 | HCID 86610107 | — |
Reaction Steps
A solution of 147 mg (0.51 mmol) of 3-chloro-5-(2-chloro-5-ethynylphenoxy)benzonitrile, 166 mg (0.48 mmol) of tert-butyl 3-iodo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate, 17 mg (0.03 mmol) of bis(triphenylphosphino)palladium (II) chloride, and 9.00 mg (0.05 mmol) of CuI in 2.5 mL DMF/5 mL triethylamine under nitrogen was stirred at room temperature for one hour. The reaction mixture was concentrated in vacuo to a dark oil. The crude oil was purified by flash chromatography over silica gel with 2.5:1 hexanes/EtOAc to provide the desired product as a yellow oil/foam. M+=405 (M−100, loss of Boc). 1H NMR (CDCl3): 1.75 (s, 9H), 7.10 (m, 1H), 7.19 (m, 1H), 7.36 (m, 1H), 7.39 (m, 2H), 7.50 (dd, 1H), 7.56 (dd, 1H), 8.21 (dd, 1H), 8.82 (dd, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807684B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-5ca82305dec94a28bf5c6f8971e1be4f |
| Source note | uspto-grants-2010_10 |