HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925294Generated: October 29, 2026
Triethylamine → 4-Methylsulfanyl-[2,2']bipyridinyl-6-carbonitrile
https://huagongshe.com/reaction/925294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | 4-Methylsulfanyl-[2,2']bipyridinyl 1-oxide | HCID 59201292 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Methylsulfanyl-[2,2']bipyridinyl-6-carbonitrile | HCID 56963376 | — |
Reaction Steps
Diethyl cyanophosphonate 90% (1.3 mL, 8.4 mmol) was slowly added at 25° C. to a mixture of 4-Methylsulfanyl-[2,2′]bipyridinyl 1-oxide (650.0 mg, 2.98 mmol) and triethylamine (0.50 mL, 3.58 mmol) in acetonitrile (14 mL) and stirred for 2 hours at 90° C. The reaction mixture was concentrated under reduced pressure, methanol (5 mL) added and the solid formed filtered and washed with methanol (2×5 mL), the filtrate was concentrated and purified by column chromatography on silica gel (0 to 10% Methanol in dichloromethane) to afford 4-methylsulfanyl-[2,2′]bipyridinyl-6-carbonitrile as a white solid that was combined with the previous white solid obtained (500.0 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284296B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-381c0377108d4ae7aafe393b01e8857e |
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| Source note | uspto-grants-2016_03 |
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