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HRID 456720作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物HexamethylenetetramineHCID 4101—
反応物2-(Benzylamino)acetic acidHCID 86965—
反応物(E)-4-((1-(3,5-Dichlorophenyl)-3-methyl-2,5-dioxoimidazolidin-4-ylidene)methyl)benzonitrileHCID 10270593—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物4-[(5S*,9R*)-7-Benzyl-3-(3,5-dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro[4.4]non-9-yl]-benzonitrileHCID 11994511—

反応条件

温度140 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07186727B2
出典データセットuspto-grants-2007_03
ORD IDord-2d6bc040ace94bfc83405eb1ce3346cd
出典メモuspto-grants-2007_03