HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl alcohol → HCID 6482390, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | HCID 11755179 | HCID 11755179 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diethylamine | HCID 8021 | — |
| Product | HCID 6482390 | HCID 6482390 | 46% |
Reaction Steps
To a suspension of N-(4-chlorobenzyl)-2-iodo-7-isopropyl-4-oxo-4,7-dihydrothieno[2,3-b]pyridine-5-carboxamide (Example No. 26) (0.717 g) in diethylamine (20 mL) is added copper iodide (0.084 g) and Pd(PPh3)2Cl2 (0.052 g) followed by addition of propargyl alcohol (0.12 mL). The reaction is stirred at rt for 18 h. The diethylamine is removed in vacuo and the resulting brown solid is purified via column chromatography (CH2Cl2:CH3OH; 98:2). Fractions homogeneous by TLC are combined and concentrated in vacuo to yield an orange solid which is recrystallized from ethanol then methanol to yield 0.281 g (46%) of the title compound as a yellow, crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06239142B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-e2e2c2d9b5a34cd997d243f84bdaa5cc |
| Source note | uspto-grants-2001_05 |