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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9460Generated: October 30, 2026

Ethyl orthoformate → HCID 21984054, compound

https://huagongshe.com/reaction/9460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant1-(3-Amino-7-benzylquinolin-4-ylamino)-2-methylpropan-2-olHCID 21984192—
Reactant1-(3-Amino-6-benzylquinolin-4-ylamino)-2-methylpropan-2-olHCID 21984362—
ProductHCID 21984054HCID 21984054—
ProductHCID 21984293HCID 21984293—

Reaction Steps

For Examples 431 and 434, a modification of the method described in Part B of Examples 427–429 was used to treat 1-(3-amino-7-benzylquinolin-4-ylamino)-2-methylpropan-2-ol or 1-(3-amino-6-benzylquinolin-4-ylamino)-2-methylpropan-2-ol with triethyl orthoformate, as indicated in the table below. The reaction was heated at reflux for one hour and then stirred overnight at ambient temperature. A precipitate formed, which was isolated by filtration to provide 1-(7-benzyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol or 1-(8-benzyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091214B2
Source datasetuspto-grants-2006_08
ORD IDord-7c4ba5b0737a4f89b2ca5ce53f1a44b3
Source noteuspto-grants-2006_08