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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621525Generated: October 27, 2026

Water → 3,4-dihydro-6-(3,4-dimethoxyphenyl)-1,3-dimethyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinone

https://huagongshe.com/reaction/621525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178418505HCID 178418505—
SolventDimethylformamideHCID 6228—
Product3,4-dihydro-6-(3,4-dimethoxyphenyl)-1,3-dimethyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinoneHCID 984353380%

Reaction Steps

To a suspension of 3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinone (1.0 g) in N,N-dimethylformamide (10 ml) were added potassium tert-butoxide (0.38 g) and methyl iodide (0.33 ml) and the mixture was stirred at ambient temperature for 5 hours. To the reaction mixture were added additional potassium tert-butoxide (0.38 g) and methyl iodide (0.17 ml) and the mixtures was stirred at ambient temperature for more 2 hours. The mixture was poured into water (100 ml) and the resulting precipitates were collected by filtration. The precipitate was recrystallized from a mixture of methanol and water (5:1) to give 3,4-dihydro-6-(3,4-dimethoxyphenyl)-1,3-dimethyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinone (0.83 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824851
Source datasetuspto-grants-1989_04
ORD IDord-edb390f4d4034375aaa3738cf1a41ee1
Source noteuspto-grants-1989_04