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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653651Generated: October 25, 2026

Bicyclo(2.2.1)heptan-2-one → 1-Methyl-5-[3-(Bicyclo[2.2.1]hept-2-ylamino)-4-Methoxyphenyl]-2-Imidazolidinone

https://huagongshe.com/reaction/653651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicyclo(2.2.1)heptan-2-oneHCID 10345—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-Methyl-5-(3-Amino-4-Methoxyphenyl)-2-ImidazolidinoneHCID 19378882—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product1-Methyl-5-[3-(Bicyclo[2.2.1]hept-2-ylamino)-4-Methoxyphenyl]-2-ImidazolidinoneHCID 1401020510.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

The aniline of Example 51 (3.07 g, 17.95 mmol) is dissolved in 60 ml of glacial acetic acid and to this is added norcamphor (2.37 g, 21.54 mmol). The reaction is cooled to 5° C. and to it is added sodium cyanoborohydride (1.36 g, 21.54 mmol). The reaction is poured onto ice and is pH adjusted to 7 with 1 normal NaOH solution. The aqueous is extracted with methylene chloride dried over MgSO4, filtered and concentrated in vacuo to afford a brown oil which is flashed on SiO2 with ethyl acetate as the eluent. The appropriate fractions are combined and concentrated in vacuo to yield a white paste which is tritarted with ether to yield 0.57 g (10%) of the product as a white crystalline solid. MP=171°-174° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05128358
Source datasetuspto-grants-1992_07
ORD IDord-13bf42b1e6354808aa135d37f62e2de0
Source noteuspto-grants-1992_07