HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373944Generated: October 31, 2026
2,2-Dimethoxypropane → HCID 21075782, compound
https://huagongshe.com/reaction/1373944
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | HCID 21075713 | HCID 21075713 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21075782 | HCID 21075782 | 100.1% |
Reaction Steps
A solution of 1H-imidazo[4,5-c]quinolin-1-amine (2.86 g, 15.5 mmol) in 60 mL of acetonitrile and 15 mL of glacial acetic acid was treated with 2,2-dimethoxypropane (9.53 mL, 77.5 mmol) and heated to 100° C. under an atmosphere of nitrogen. After 18 h, the reaction mixture was concentrated under reduced pressure to give a brown oil. The oil was dissolved in 100 mL of CHCl3 and washed with 5% Na2CO3 solution (2×30 mL), water (30 mL) and brine (30 mL). The organic portion was dried over Na2SO4, filtered and concentrated under reduced pressure to yield 3.48 g of N-(1H-imidazo[4,5-c]quinolin-1-yl)isopropylideneamine as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07163947B2 |
|---|
| Source dataset | uspto-grants-2007_01 |
|---|
| ORD ID | ord-e559613019ad4aeba8ff7dcf318d1763 |
|---|
| Source note | uspto-grants-2007_01 |
|---|