HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798513Generated: October 29, 2026
Potassium Carbonate → Cyclopropyl-(5''-ethynyl-[2,2';4',3'']terpyridin-6'-yl)-amine
https://huagongshe.com/reaction/1798513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Cyclopropyl-(5''-trimethylsilanylethynyl-[2,2';4',3'']terpyridin-6'-yl)-amine | HCID 68947114 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Cyclopropyl-(5''-ethynyl-[2,2';4',3'']terpyridin-6'-yl)-amine | HCID 86633651 | — |
Reaction Steps
Cyclopropyl-(5″-trimethylsilanylethynyl-[2,2′;4′,3″]terpyridin-6′-yl)-amine (Example 2.128, step1) (1 eq, 0.127 mmol, 49 mg) is dissolved in MeOH (2 ml) and potassium carbonate is added (2 eq, 0.255 mmol, 35 mg). The reaction mixture is dissolved in EtOAc and washed with water. The organic layer is washed with brine, dried over drying agent MgSO4, filtered and the organic solvent is reduced in vacuo. The crude residue is purified by reverse phase column chromatography (Isolute™ C18, 0-20% acetonitrile in water—0.1% TFA). The appropriate fractions by HPLC are combined and concentrated in vacuo. The resulting residue is dissolved in MeOH and loaded onto a SCX-2 cartridge eluting with MeOH followed by 2M NH3 in MeOH. The methanolic ammonia fractions are combined, concentrated in vacuo and dried under vacuum to afford the title compound; [M+H]+ 313.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08343966B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-7cb0218a28bb47e693f9f4cb5729e5ee |
|---|
| Source note | uspto-grants-2013_01 |
|---|