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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366727Generated: November 1, 2026

Trimethyl orthovalerate → HCID 69506740, compound

https://huagongshe.com/reaction/2366727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthovalerateHCID 83755—
Reactant1,1,1-TrimethoxybutaneHCID 123512—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantHCID 57447056HCID 57447056—
ProductHCID 69506740HCID 69506740—

Reaction Steps

Ethyl 3-(3-aminoquinolin-4-ylamino)-2,2-dimethylpropanoate (see Example 26 Parts A through D, 9.0 g, 31.3 mmol) was treated according to a modification of the method described in Part B of Example 8 using trimethyl orthovalerate in lieu of trimethyl orthobutyrate. Prior to the addition of trimethyl orthovalerate (6.1 mL, 35 mmol) and pyridinium p-toluenesulfonate (0.050 g), the reaction was heated at reflux for 15 minutes and then cooled slightly. The reaction was heated at reflux for five hours, allowed to cool to ambient temperature, stirred overnight, and concentrated under reduced pressure to provide 11.2 g of ethyl 3-(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)-2,2-dimethylpropanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697873B2
Source datasetuspto-grants-2014_04
ORD IDord-a73e0d67db6149efa61dd8c8aba3282b
Source noteuspto-grants-2014_04