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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36471Generated: October 27, 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/36471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicyclo(2.2.1)heptan-2-oneHCID 10345—
ReactantSodium HydroxideHCID 14798—
ReactantCyano-borohydrideHCID 498716—
ReactantSodiumHCID 5360545—
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 14010205—

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 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 numberUS05414127
Source datasetuspto-grants-1995_05
ORD IDord-12b77248c78349309b3b268a58c4f4f8
Source noteuspto-grants-1995_05