HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl orthoacetate → HCID 21075820, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl orthoacetate | HCID 15050 | — |
| Reactant | tert-butyl N'-(3-aminoquinolin-4-yl)hydrazinecarboxylate | HCID 21075823 | — |
| Reactant | Ethylacetate methanol | HCID 21584119 | — |
| Catalyst | Pyridinium chloride | HCID 10176127 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21075820 | HCID 21075820 | 84.4% |
Reaction Steps
A solution of tert-butyl N′-(3-aminoquinolin-4-yl)hydrazinecarboxylate (11.67 g, 42.5 mmol) in 400 mL of anhydrous toluene was treated with trimethyl orthoacetate (5.96 mL, 46.8 mmol) and pyridine hydrochloride (100 mg) under an atmosphere of N2 and heated to reflux. After stirring for 3 h, the reaction mixture was concentrated under reduced pressure to give a red solid. Chromatography (SiO2, 0–10% MeOH/EtOAc) gave tert-butyl N-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)carbamate (10.7 g) as a yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07163947B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-4698ee159fcf4389a15ee02da25f4d4c |
| Source note | uspto-grants-2007_01 |