HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminopyridine-3-carbonitrile → HCID 178507213, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminopyridine-3-carbonitrile | HCID 577016 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 178470777 | HCID 178470777 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178507213 | HCID 178507213 | — |
Reaction Steps
LiHMDS (3.3 eq) was added to ethyl (5-morpholin-4-yl-1H-benzimidazol-2-yl)acetate (1.0 eq) and 4-aminopyridine-3-carbonitrile (see J. Chem. Soc. 1967, p 1558–1564; 1.0 eq) in THF at 0° C. The reaction was stirred overnight. The resulting mixture was quenched with an aqueous saturated NH4Cl solution and extracted with EtOAc. The combined organic layers were washed with H2O and brine, dried over Na2SO4, filtered, and concentrated in vacuo to yield a brown solid. The crude material was washed successively with CH2Cl2 and MeOH, and then was purified by reverse phase HPLC to provide the desired product. LC/MS m/z 363.2 (MH+), Rt 1.55 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138409B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-45f647adc99b4c9ba34a40f6999ae76e |
| Source note | uspto-grants-2006_11 |