HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264523Generated: October 26, 2026
Benzyl Alcohol → N-{4-[2-Amino-6-(benzyloxy)-3,5-dicyano-4-pyridinyl]phenyl}acetamide
https://huagongshe.com/reaction/2264523
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-{4-[2-Amino-3,5-dicyano-6-(phenylsulphanyl)-4-pyridinyl]phenyl}acetamide | HCID 12016387 | — |
| Product | N-{4-[2-Amino-6-(benzyloxy)-3,5-dicyano-4-pyridinyl]phenyl}acetamide | HCID 10221564 | — |
Reaction Steps
58 mg (0.15 mmol) of N-{4-[2-amino-3,5-dicyano-6-(phenylsulfanyl)-4-pyridinyl]phenyl}acetamide [prepared analogously to Kambe et al., Synthesis, 531-533 (1981)] are, together with 41 mg (0.3 mmol) of potassium carbonate, dissolved/suspended in 1.88 g (=1.8 ml, 17.4 mmol) of benzyl alcohol, and the mixture is stirred at 100° C. for 3.5 h. The benzyl alcohol is evaporated under reduced pressure and the evaporation residue is purified by preparative HPLC on reversed-phase silica gel (gradient: water/acetonitrile 90:1010:90 in 38 minutes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855219B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-6a6345a0e9c445b8ae3a4ec1262644f8 |
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| Source note | uspto-grants-2010_12 |
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