HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 21075790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 69177440 | HCID 69177440 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21075790 | HCID 21075790 | 90.8% |
Reaction Steps
A solution of N-(2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)(furan-2-ylmethylene)amine (1.86 g, 5.81 mmol) in 20 mL of methanol was treated with NaBH4 (0.659 g, 17.4 mmol) and stirred under an atmosphere of nitrogen. After 18 h the reaction was quenched by addition of 20 mL of water. The reaction mixture was concentrated under reduced pressure and dissolved in CHCl3. The organic portion was washed with 2% Na2CO3 solution, water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure to yield N-(2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)(furan-2-ylmethyl)amine (1.70 g) as a thick orange syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07163947B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-e00c4c06eead4bacba633652b4748d8b |
| Source note | uspto-grants-2007_01 |