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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34654Generated: October 29, 2026

Potassium Carbonate → (+/-) trans-(5,6,6a,7,8,9,10,10a-Octahydro-7-propylpyrido[2,3-h]quinazolin-2-yl)-carbamic acid, phenylmethyl ester

https://huagongshe.com/reaction/34654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodopropaneHCID 33643—
Reactant(+/-) trans-(5,6,6a,7,8,9,10,10a-Octahydropyrido[2,3-h]quinazolin-2-yl)-carbamic acid, phenylmethyl esterHCID 14233853—
SolventAcetonitrileHCID 6342—
ProductAmmonium HydroxideHCID 14923—
Product(+/-) trans-(5,6,6a,7,8,9,10,10a-Octahydro-7-propylpyrido[2,3-h]quinazolin-2-yl)-carbamic acid, phenylmethyl esterHCID 14233855144.2%

Reaction Steps

A mixture of 1.74 g (5.14 mmol) of (±) trans-(5,6,6a,7,8,9,10,10a-octahydropyrido[2,3-h]quinazolin-2-yl)-carbamic acid, phenylmethyl ester, (Example 20), 3.6 g (26.05 mmol) of finely ground potassium carbonate and 2.5 ml (25.63 mmol) of 1-iodopropane in 250 ml acetonitrile is refluxed, under nitrogen, for 24 hours. The suspension is cooled, filtered through a pad of Celite, concentrated and partitioned between brine and chloroform. The chloroform extract is separated, dried over magnesium sulfate, filtered and concentrated to a viscous brown oil. Medium pressure chromatography (silica gel, 2% ammonium hydroxide-98% ethyl acetate) afforded 1.41 g (72%) of the title compound as a white solid; mp 174°-177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04762843
Source datasetuspto-grants-1988_08
ORD IDord-c0673a36ea004128ba9aff88e2e2c5b8
Source noteuspto-grants-1988_08