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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456720Generated: October 25, 2026

Toluene → 4-[(5S*,9R*)-7-Benzyl-3-(3,5-dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro[4.4]non-9-yl]-benzonitrile

https://huagongshe.com/reaction/456720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantHexamethylenetetramineHCID 4101—
Reactant2-(Benzylamino)acetic acidHCID 86965—
Reactant(E)-4-((1-(3,5-Dichlorophenyl)-3-methyl-2,5-dioxoimidazolidin-4-ylidene)methyl)benzonitrileHCID 10270593—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-[(5S*,9R*)-7-Benzyl-3-(3,5-dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro[4.4]non-9-yl]-benzonitrileHCID 11994511—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of (E)-4-((1-(3,5-dichlorophenyl)-3-methyl-2,5-dioxoimidazolidin-4-ylidene)methyl)benzonitrile (1.05 g, 2.82 mmol), hexamethylenetetramine (0.395 g, 2.82 mmol), N-benzylglycine (1.17 g, 7.05 mmol), toluene (5 ml), and 1-methyl-2-pyrrolidinone (NMP, 10 ml) was heated to 140° C. The extent of reaction was monitored by HPLC. After 72 hours, the reaction had stopped short of completion. The ratio of product to starting material ((E)-4-((1-(3,5-dichlorophenyl)-3-methyl-2,5-dioxoimidazolidin-4-ylidene)methyl)benzonitrile) was 1.36:1. Mass spectra of the mixture indicated the presence of the desired product. The mixture was washed with water and extracted into toluene. The impure product was obtained as an oil. Comparison of the product obtained to authentic material was made by HPLC. The ratio of the desired (5S, 9R) isomer to the undesired was 19:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186727B2
Source datasetuspto-grants-2007_03
ORD IDord-2d6bc040ace94bfc83405eb1ce3346cd
Source noteuspto-grants-2007_03