HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798505Generated: October 29, 2026
Acetonitrile → N-[1-(5''-Bromo-[2,2';4',3'']terpyridin-6'-yl)-1-methyl-ethyl]-acetamide
https://huagongshe.com/reaction/1798505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(5''-Bromo-[2,2';4',3'']terpyridin-6'-yl)-propan-2-ol | HCID 68735197 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[1-(5''-Bromo-[2,2';4',3'']terpyridin-6'-yl)-1-methyl-ethyl]-acetamide | HCID 68733910 | — |
Reaction Steps
To a solution of 2-(5″-Bromo-[2,2′;4′,3″]terpyridin-6′-yl)-propan-2-ol (Example 2.80; step1) (1 eq, 0.135 mmol, 50 mg) in acetonitrile (2 ml) is added tetrafluoroboric acid diethyl ether complex (3.5 eq, 0.473 mmol, 0.06 ml) and the reaction mixture is heated at 85° C. overnight. The pH of the reaction mixture is adjusted to 8-9 by addition of sodium hydroxide (2M). The solution is dissolved in DCM and washed with water. The combined organic extracts are washed with brine, dried over MgSO4 and concentrated in vacuo to afford the title compound; [M+H]+ 411/413
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-e564add6a80b4a4089ac927f528a45f2 |
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| Source note | uspto-grants-2013_01 |
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