HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383091Generated: October 29, 2026
Triethyl orthoacetate → 7-benzyloxy-2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline
https://huagongshe.com/reaction/2383091
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl orthoacetate | HCID 66221 | — |
| Reactant | 7-benzyloxy-N4-(2-methylpropyl)quinoline-3,4-diamine | HCID 67050970 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 7-benzyloxy-2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline | HCID 67050918 | — |
Reaction Steps
The preparation of 7-benzyloxy-N4-(2-methylpropyl)quinoline-3,4-diamine is described in Parts A-F of Example 1. Under a nitrogen atmosphere, triethyl orthoacetate (4.59 mL, 25.0 mmol) was added to a solution of 7-benzyloxy-N4-(2-methylpropyl)quinoline-3,4-diamine (8.05 g, 25.0 mmol) in xylenes (130 mL), and the resulting solution was heated at reflux (160° C.) overnight. The solvent volume was reduced to 70 mL using a Dean-Stark trap. Over a period of a few days, a precipitate formed. Diethyl ether was added, and the precipitate was isolated by filtration and washed with diethyl ether to provide 6.81 g of 7-benzyloxy-2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline as a light-brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263594B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-870b29a59767419f9fd33824d5679c03 |
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| Source note | uspto-grants-2012_09 |
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