HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798495Generated: October 31, 2026
Tert-Butyl-[5''-(3-methoxy-phenyl)-[2,2';4',3'']terpyridin-6'-yl]-amine → 5''-(3-Methoxy-phenyl)-[2,2';4',3'']terpyridin-6'-ylamine
https://huagongshe.com/reaction/1798495
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butyl-[5''-(3-methoxy-phenyl)-[2,2';4',3'']terpyridin-6'-yl]-amine | HCID 68736706 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5''-(3-Methoxy-phenyl)-[2,2';4',3'']terpyridin-6'-ylamine | HCID 44137102 | — |
Reaction Steps
Tert-Butyl-[5″-(3-methoxy-phenyl)-[2,2′;4′,3″]terpyridin-6′-yl]-amine (1 eq, 0.073 mmol, 0.030 g) is dissolved in TFA (6 ml)/DCM (1 ml) and the reaction mixture is heated at 70° C. for 5 hours. The reaction mixture is cooled down and reduced 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]+ 355.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343966B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-9a57e2d39c1f4cbb98d2b27e7b90135d |
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| Source note | uspto-grants-2013_01 |
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